FCC ID Z7A-SDMAC
SDIO Wireless Module
by Stryker Medical
Grantee Code: Z7A Product Code: SDMAC
Latest application date: 2018-04-26
FCC ID Device Details
| FCC ID | Z7A-SDMAC |
|---|---|
| Mirrors | fcc.id | gov | fccid.ai |
| Grantee Code | Z7A |
| Product Code | SDMAC |
| Applicant Business | Stryker Medical 🇺🇸 |
| Related Domains | |
| Equipment Class | SDIO Wireless Module |
| Test Firm | Bureau Veritas Consumer Products Services, Inc. |
Operating Frequencies
| Frequency Range | Application Purpose | Final Action Date |
|---|---|---|
| 2412-2462 MHz | Class II permissive change or modification of presently authorized equipment | 2018-04-26 |
| 5180-5240 MHz | Class II permissive change or modification of presently authorized equipment | 2018-04-26 |
| 5180-5240 MHz | Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAC Grant Date: 11/08/2016 | 2018-04-11 |
| 2412-2462 MHz | Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAC Grant Date: 11/08/2016 | 2018-04-11 |
Exhibits
| Document | Type | Available | File |
|---|---|---|---|
| Host Internal Photos | Internal Photos | 2018-04-26 | PDF 562.2 KB |
| Host External Photos | External Photos | 2018-04-26 | PDF 271.2 KB |
| External Photos | External Photos | 2018-04-11 | PDF 400.6 KB |
| Product Label | ID Label/Location Info | 2018-04-11 | PDF 520.6 KB |
| Test Setup Photos | Test Report | 2018-04-26 | PDF 171.2 KB |
| Test Setup Photos | Test Setup Photos | 2018-04-26 | PDF 500.4 KB |
| SAR Test Report Part 1 | RF Exposure Info | 2018-04-26 | PDF 3.7 MB |
| SAR Test Report Part 2 | RF Exposure Info | 2018-04-26 | PDF 4.5 MB |
| Class II Permissive Change Letter | Cover Letter(s) | 2018-04-26 | PDF 500.4 KB |
| Class II Permissive Change Letter | Cover Letter(s) | 2018-04-26 | PDF 793.2 KB |
| Product Certification Representative Auth Letter | Cover Letter(s) | 2018-04-26 | PDF 793.2 KB |
| Change of ID Auth Letter | Cover Letter(s) | 2018-04-11 | PDF 147.2 KB |
| Change of ID Request Letter | Cover Letter(s) | 2018-04-11 | PDF 212.3 KB |
| Product Certification Representative Auth Letter | Cover Letter(s) | 2018-04-11 | PDF 790 KB |
Application Information
| Application ID | KMgyaeIu8M2PoelPNvER2w== |
|---|---|
| Final Action Date | 2018-04-26 |
| Application Purpose | Class II permissive change or modification of presently authorized equipment |
| Applicant FRN | 0021243142 |
| Model | SDMAC |
| Frequency Range | 2412-2462 MHz |
| Equipment Class | DTS - Digital Transmission System |
| Device Description | SDIO Wireless Module |
| Responsible Party | Michael Hayes, Sr Principle EE, mike.hayes@stryker.com |
| Test Firm | Sarb Shelopal, Bureau Veritas Consumer Products Services, Inc., Sarbjit.Shelopal@bureauveritas.com |
| TCB Email | tcb@siemic.com |
| TCB Scope | A4: UNII devices & low power transmitters using spread spectrum techniques |
| Short-Term Confidentiality | No |
| Long-Term Confidentiality | No |
| Grant Deferral | No |
| Modular Equipment | Single Modular Approval |
| Composite Device | Yes |
| Composite Part | No |
| Cognitive Radio | No |
| Authorization Waiver | No |
| Authorization Waiver Approved | No |
| Section 5301 Certification | Yes |
| Related OET Knowledge DataBase Inquiry | No |
| Grant Comments | C2PC to add portable SAR when used in Stryker InTouch Bed Control Panel host. The highest reported SAR value found during evaluation is: Body: 0.33 W/kg Original grant comment: Single Modular Approval. Output power listed is Conducted(Peak). For professional installation only. Device shall not be sold to general public. This device has a 20 MHz and 40 MHz bandwidth mode. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter except the conditions shown in this filing and/or in accordance with FCC multi-transmitter product guidelines. OEM integrators must be provided with antenna installation instructions. |
Applications
| Application ID | Date | Purpose |
|---|---|---|
| KMgyaeIu8M2PoelPNvER2w== | 2018-04-26 | Class II permissive change or modification of presently authorized equipment |
| 4RY/Ajmr3TfQ1cJ7jxz+8A== | 2018-04-26 | Class II permissive change or modification of presently authorized equipment |
| U4q2xhkF+hK55g9PkAdIjA== | 2018-04-11 | Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAC Grant Date: 11/08/2016 |
| 0V7RqOpJdw7RvOz6pK0NGg== | 2018-04-11 | Change in identification of presently authorized equipment. Original FCC ID: N6C-SDMAC Grant Date: 11/08/2016 |
Equipment Authorization
Grants
TCB Grant - Application U4q2xhkF+hK55g9PkAdIjA==
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
Bureau Veritas Consumer Products Services, Inc. 775 Montague Expressway Milpitas, CA 95035 |
Date of Grant: 04/11/2018 Application Dated: 04/11/2018 |
| Stryker Medical |
| 3800 East Centre Ave |
| Portage, MI 49002 |
| Attention: Michael Hayes , Sr Principle EE |
| NOT TRANSFERABLE |
| EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below. |
| FCC IDENTIFIER: | Z7A-SDMAC |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | SDIO Wireless Module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15E | 5180.0 - 5240.0 | 0.0251 | ||
| CC ND | 15E | 5260.0 - 5320.0 | 0.0251 | ||
| CC ND | 15E | 5500.0 - 5700.0 | 0.009 | ||
| CC | 15E | 5745.0 - 5825.0 | 0.0139 |
| Single Modular Approval. Output power listed is Conducted. For professional installation only. Device shall not be sold to general public. This device has a 20 MHz, 40 MHz and 80 MHz bandwidth mode for 5 GHz bands. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter except the conditions shown in this filing and/or in accordance with FCC multi-transmitter product guidelines. OEM integrators must be provided with antenna installation instructions. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and KDB 905462 D01 as a Client only without Radar Detection. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
| ND: | This UNII device complies with the Transmit Power Control (TPC) and Dynamic Frequency Selection (DFS) requirements in Section 15.407(h). |
EAS Grant - Application U4q2xhkF+hK55g9PkAdIjA==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
Stryker Medical 3800 East Centre Ave P.O. Box , Portage, MI 49002 United States |
Date of Grant: 04/11/2018 Application Dated: 04/11/2018 |
| Attention: Michael Hayes , Sr Principle EE |
| NOT TRANSFERABLE |
| EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below. |
| FCC IDENTIFIER: | Z7A-SDMAC |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | SDIO Wireless Module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15E | 5180.0 - 5240.0 | 0.0251 | ||
| CC ND | 15E | 5260.0 - 5320.0 | 0.0251 | ||
| CC ND | 15E | 5500.0 - 5700.0 | 0.009 | ||
| CC | 15E | 5745.0 - 5825.0 | 0.0139 |
| Single Modular Approval. Output power listed is Conducted. For professional installation only. Device shall not be sold to general public. This device has a 20 MHz, 40 MHz and 80 MHz bandwidth mode for 5 GHz bands. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter except the conditions shown in this filing and/or in accordance with FCC multi-transmitter product guidelines. OEM integrators must be provided with antenna installation instructions. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and KDB 905462 D01 as a Client only without Radar Detection. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
| ND: | This UNII device complies with the Transmit Power Control (TPC) and Dynamic Frequency Selection (DFS) requirements in Section 15.407(h). |
| Mail To: | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
Bureau Veritas Consumer Products Services, Inc. 775 Montague Expressway Milpitas, CA 95035 |
Date of Grant: 04/26/2018 Application Dated: 04/26/2018 |
| Stryker Medical |
| 3800 East Centre Ave |
| Portage, MI 49002 |
| Attention: Michael Hayes , Sr Principle EE |
| NOT TRANSFERABLE |
| EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below. |
| FCC IDENTIFIER: | Z7A-SDMAC |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | SDIO Wireless Module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2412.0 - 2462.0 | 0.2999 |
| C2PC to add portable SAR when used in Stryker InTouch Bed Control Panel host. The highest reported SAR value found during evaluation is: Body: 0.33 W/kg Original grant comment: Single Modular Approval. Output power listed is Conducted(Peak). For professional installation only. Device shall not be sold to general public. This device has a 20 MHz and 40 MHz bandwidth mode. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter except the conditions shown in this filing and/or in accordance with FCC multi-transmitter product guidelines. OEM integrators must be provided with antenna installation instructions. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
EAS Grant - Application KMgyaeIu8M2PoelPNvER2w==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
Stryker Medical 3800 East Centre Ave P.O. Box , Portage, MI 49002 United States |
Date of Grant: 04/26/2018 Application Dated: 04/26/2018 |
| Attention: Michael Hayes , Sr Principle EE |
| NOT TRANSFERABLE |
| EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below. |
| FCC IDENTIFIER: | Z7A-SDMAC |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | SDIO Wireless Module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2412.0 - 2462.0 | 0.2999 |
| C2PC to add portable SAR when used in Stryker InTouch Bed Control Panel host. The highest reported SAR value found during evaluation is: Body: 0.33 W/kg Original grant comment: Single Modular Approval. Output power listed is Conducted(Peak). For professional installation only. Device shall not be sold to general public. This device has a 20 MHz and 40 MHz bandwidth mode. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter except the conditions shown in this filing and/or in accordance with FCC multi-transmitter product guidelines. OEM integrators must be provided with antenna installation instructions. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
| Mail To: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
Bureau Veritas Consumer Products Services, Inc. 775 Montague Expressway Milpitas, CA 95035 |
Date of Grant: 04/26/2018 Application Dated: 04/26/2018 |
| Stryker Medical |
| 3800 East Centre Ave |
| Portage, MI 49002 |
| Attention: Michael Hayes , Sr Principle EE |
| NOT TRANSFERABLE |
| EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below. |
| FCC IDENTIFIER: | Z7A-SDMAC |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | SDIO Wireless Module |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15E | 5180.0 - 5240.0 | 0.0251 | ||
| CC ND | 15E | 5260.0 - 5320.0 | 0.0251 | ||
| CC ND | 15E | 5500.0 - 5700.0 | 0.009 | ||
| CC | 15E | 5745.0 - 5825.0 | 0.0139 |
| C2PC to add portable SAR when used in Stryker InTouch Bed Control Panel host. The highest reported SAR value found during evaluation is: Body: 0.33 W/kg Original grant comment: Single Modular Approval. Output power listed is Conducted. For professional installation only. Device shall not be sold to general public. This device has a 20 MHz, 40 MHz and 80 MHz bandwidth mode for 5 GHz bands. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter except the conditions shown in this filing and/or in accordance with FCC multi-transmitter product guidelines. OEM integrators must be provided with antenna installation instructions. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and KDB 905462 D01 as a Client only without Radar Detection. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
| ND: | This UNII device complies with the Transmit Power Control (TPC) and Dynamic Frequency Selection (DFS) requirements in Section 15.407(h). |
EAS Grant - Application 4RY/Ajmr3TfQ1cJ7jxz+8A==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
Stryker Medical 3800 East Centre Ave P.O. Box , Portage, MI 49002 United States |
Date of Grant: 04/26/2018 Application Dated: 04/26/2018 |
| Attention: Michael Hayes , Sr Principle EE |
| NOT TRANSFERABLE |
| EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below. |
| FCC IDENTIFIER: | Z7A-SDMAC |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Unlicensed National Information Infrastructure TX |
| Notes: | SDIO Wireless Module |
| Modular Type: | Does not apply |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15E | 5180.0 - 5240.0 | 0.0251 | ||
| CC ND | 15E | 5260.0 - 5320.0 | 0.0251 | ||
| CC ND | 15E | 5500.0 - 5700.0 | 0.009 | ||
| CC | 15E | 5745.0 - 5825.0 | 0.0139 |
| C2PC to add portable SAR when used in Stryker InTouch Bed Control Panel host. The highest reported SAR value found during evaluation is: Body: 0.33 W/kg Original grant comment: Single Modular Approval. Output power listed is Conducted. For professional installation only. Device shall not be sold to general public. This device has a 20 MHz, 40 MHz and 80 MHz bandwidth mode for 5 GHz bands. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter except the conditions shown in this filing and/or in accordance with FCC multi-transmitter product guidelines. OEM integrators must be provided with antenna installation instructions. This device complies with the Dynamic Frequency Selection (DFS) requirements of Report and KDB 905462 D01 as a Client only without Radar Detection. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
| ND: | This UNII device complies with the Transmit Power Control (TPC) and Dynamic Frequency Selection (DFS) requirements in Section 15.407(h). |
| Mail To: | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
Bureau Veritas Consumer Products Services, Inc. 775 Montague Expressway Milpitas, CA 95035 |
Date of Grant: 04/11/2018 Application Dated: 04/11/2018 |
| Stryker Medical |
| 3800 East Centre Ave |
| Portage, MI 49002 |
| Attention: Michael Hayes , Sr Principle EE |
| NOT TRANSFERABLE |
| EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below. |
| FCC IDENTIFIER: | Z7A-SDMAC |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | SDIO Wireless Module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2412.0 - 2462.0 | 0.2999 |
| Single Modular Approval. Output power listed is Conducted(Peak). For professional installation only. Device shall not be sold to general public. This device has a 20 MHz and 40 MHz bandwidth mode. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter except the conditions shown in this filing and/or in accordance with FCC multi-transmitter product guidelines. OEM integrators must be provided with antenna installation instructions. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
EAS Grant - Application 0V7RqOpJdw7RvOz6pK0NGg==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
Stryker Medical 3800 East Centre Ave P.O. Box , Portage, MI 49002 United States |
Date of Grant: 04/11/2018 Application Dated: 04/11/2018 |
| Attention: Michael Hayes , Sr Principle EE |
| NOT TRANSFERABLE |
| EQUIPMENT AUTHORIZATION is hereby issued to the named GRANTEE, and is VALID ONLY for the equipment identified hereon for use under the Commission's Rules and Regulations listed below. |
| FCC IDENTIFIER: | Z7A-SDMAC |
| Name of Grantee: | Stryker Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | SDIO Wireless Module |
| Modular Type: | Single Modular |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| CC | 15C | 2412.0 - 2462.0 | 0.2999 |
| Single Modular Approval. Output power listed is Conducted(Peak). For professional installation only. Device shall not be sold to general public. This device has a 20 MHz and 40 MHz bandwidth mode. Separate evaluation must be required for any portable configuration. When used in mobile applications, the antennas shown in this filing must be installed to provide a separation distance of at least 20 cm from all persons. Compliance of this device in all final host configurations is the responsibility of the Grantee. OEM integrators and end-users must be provided with specific information required to satisfy RF exposure compliance for the final host device. OEM integrators are instructed to ensure that the end user has no manual instructions to remove or install the device. The antenna of this device must not be co-located or used in conjunction with any other antenna or transmitter except the conditions shown in this filing and/or in accordance with FCC multi-transmitter product guidelines. OEM integrators must be provided with antenna installation instructions. |
| CC: | This device is certified pursuant to two different Part 15 rules sections. |
| Mail To: |