FCC ID RIAICDRFNGQ
Implantable Cardioverter Defibrillator Device
by St. Jude Medical
Grantee Code: RIA Product Code: ICDRFNGQ
Latest application date: 2024-08-01
FCC ID Device Details
Linked Records
Barcode records decoded from published FCC label exhibits or linked by an explicit FCC ID reference on a product page.
| UPC / GTIN | Linked product |
|---|---|
| 5414734505666 EAN-13 · GTIN-14 05414734505666 | Implantable Cardioverter Defibrillator Device Brand: St. Jude Medical · Model: ICDRFNGQ Source: FCC label |
| 5415067032843 EAN-13 · GTIN-14 05415067032843 | Implantable Cardioverter Defibrillator Device Brand: St. Jude Medical · Model: ICDRFNGQ Source: FCC label |
| 5415067032850 EAN-13 · GTIN-14 05415067032850 | Implantable Cardioverter Defibrillator Device Brand: St. Jude Medical · Model: ICDRFNGQ Source: FCC label |
Operating Frequencies
| Frequency Range | Application Purpose | Final Action Date |
|---|---|---|
| 2402-2480 MHz | Class II permissive change or modification of presently authorized equipment | 2024-08-01 |
| 2402-2480 MHz | Class II permissive change or modification of presently authorized equipment | 2023-07-27 |
| 2402-2480 MHz | Original Equipment | 2019-10-18 |
Exhibits
| Document | Type | Available | File |
|---|---|---|---|
| User Manual | Users Manual | 2024-01-10 | PDF 4.9 MB |
| User Manual | Users Manual | 2020-04-10 | PDF 1.3 MB |
| Internal Photos | Internal Photos | 2020-04-10 | PDF 111.5 KB |
| External Photos | External Photos | 2024-08-01 | PDF 2.2 MB |
| External Photos | External Photos | 2024-01-10 | PDF 227.4 KB |
| External photos | External Photos | 2020-04-10 | PDF 96.1 KB |
| Label | ID Label/Location Info | 2024-08-01 | PDF 3.3 MB |
| Label | ID Label/Location Info | 2023-07-27 | PDF 2.5 MB |
| Label 1 | ID Label/Location Info | 2019-10-18 | PDF 388.4 KB |
| Label 10 | ID Label/Location Info | 2019-10-18 | PDF 388.1 KB |
| Label 12 | ID Label/Location Info | 2019-10-18 | PDF 382.3 KB |
| Label 13 | ID Label/Location Info | 2019-10-18 | PDF 388.9 KB |
| Label 14 | ID Label/Location Info | 2019-10-18 | PDF 387.5 KB |
| Label 15 | ID Label/Location Info | 2019-10-18 | PDF 388.8 KB |
| Label 2 | ID Label/Location Info | 2019-10-18 | PDF 387 KB |
| Label 3 | ID Label/Location Info | 2019-10-18 | PDF 381.3 KB |
| Label 4 | ID Label/Location Info | 2019-10-18 | PDF 391.8 KB |
| Label 5 | ID Label/Location Info | 2019-10-18 | PDF 385.8 KB |
| Label 6 | ID Label/Location Info | 2019-10-18 | PDF 381.1 KB |
| Label 7 | ID Label/Location Info | 2019-10-18 | PDF 389.3 KB |
| Label 8 | ID Label/Location Info | 2019-10-18 | PDF 386 KB |
| Label 9 | ID Label/Location Info | 2019-10-18 | PDF 382 KB |
| Lable 11 | ID Label/Location Info | 2019-10-18 | PDF 389.8 KB |
| Test Setup Photos | Test Setup Photos | 2024-08-01 | PDF 2.1 MB |
| Test Setup Photos | Test Setup Photos | 2024-01-10 | PDF 1.6 MB |
| Test Setup Photos | Test Setup Photos | 2020-04-10 | PDF 718.1 KB |
| Antenna Information | Test Report | 2024-08-01 | PDF 62.7 KB |
| Test Report | Test Report | 2024-08-01 | PDF 5.8 MB |
| Test Report | Test Report | 2023-07-27 | PDF 3.8 MB |
| Test Report | Test Report | 2019-10-18 | PDF 2.9 MB |
| Attestation Statements US agent for service of process | Attestation Statements | 2024-08-01 | PDF 65.1 KB |
| Attestation of Covered Equipment | Attestation Statements | 2024-08-01 | PDF 19 KB |
| 2.911 (d)(5)(i)-(ii) Covered equipment attestation | Attestation Statements | 2023-07-27 | PDF 19 KB |
| 2.911 (d)(7) Attestation Statements US agent for service | Attestation Statements | 2023-07-27 | PDF 65.1 KB |
| Agency Letter | Cover Letter(s) | 2024-08-01 | PDF 22.1 KB |
| C2PC Letter | Cover Letter(s) | 2024-08-01 | PDF 45.8 KB |
| Models Difference Letter | Cover Letter(s) | 2024-08-01 | PDF 85.7 KB |
| Antenna Information | Cover Letter(s) | 2023-07-27 | PDF 94.4 KB |
| C2PC Letter | Cover Letter(s) | 2023-07-27 | PDF 15.7 KB |
| Confidentiality Letter | Cover Letter(s) | 2023-07-27 | PDF 31 KB |
| Model difference Letter | Cover Letter(s) | 2023-07-27 | PDF 88.1 KB |
| Agent letter | Cover Letter(s) | 2019-10-18 | PDF 51.9 KB |
| Confidentiality Letter | Cover Letter(s) | 2019-10-18 | PDF 80.8 KB |
| Family Application Letter | Cover Letter(s) | 2019-10-18 | PDF 184.9 KB |
| RF Exposure Report | RF Exposure Info | 2024-08-01 | PDF 171.4 KB |
| RF Exposure Report | RF Exposure Info | 2023-07-27 | PDF 253.6 KB |
| RF Exposure Report | RF Exposure Info | 2019-10-18 | PDF 199.8 KB |
| Block Diagram Metadata only | Block Diagram | PDF 53.9 KB | |
| Schematics Metadata only | Schematics | PDF 98.2 KB | |
| Operating Description Metadata only | Operational Description | PDF 27.6 KB |
Application Information
| Application ID | XMouVUDe+y8Yf3soVK42Ww== |
|---|---|
| Final Action Date | 2024-08-01 |
| Application Purpose | Class II permissive change or modification of presently authorized equipment |
| Applicant FRN | 0028172476 |
| Model | ICDRFNGQ |
| Frequency Range | 2402-2480 MHz |
| Equipment Class | DTS - Digital Transmission System |
| Device Description | Implantable Cardioverter Defibrillator Device |
| Responsible Party | Jennifer A Wong, Director, Regulatory Affairs, jwong03@sjm.com |
| Test Firm | Mac Elliott, TUV SUD America Inc., William.Elliott@tuvsud.com |
| TCB Email | andy.zhang@tuvsud.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 | Does not apply |
| Composite Device | No |
| 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 as describe in this filling. Output power is conducted. |
Applications
| Application ID | Date | Purpose |
|---|---|---|
| XMouVUDe+y8Yf3soVK42Ww== | 2024-08-01 | Class II permissive change or modification of presently authorized equipment |
| mWEBVBkUk+XKSrkzdbxOcQ== | 2023-07-27 | Class II permissive change or modification of presently authorized equipment |
| nAEwg/RruycIoqYDk5emMg== | 2019-10-18 | Original Equipment |
Equipment Authorization
| Frequency | Output | Rules |
|---|---|---|
| 2402-2480 MHz | 0.0020000 | 15C |
Grants
TCB Grant - Application XMouVUDe+y8Yf3soVK42Ww==
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
TUV SUD America Inc. 401 Edgewater Place Suite #500 Wakefield, MA 01880 |
Date of Grant: 08/01/2024 Application Dated: 08/01/2024 |
| St. Jude Medical |
| 15900 Valley View Court |
| Sylmar, CA 91342 |
| Attention: Jennifer Wong , Director, Regulatory Affairs |
| 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: | RIAICDRFNGQ |
| Name of Grantee: | St. Jude Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | Implantable Cardioverter Defibrillator Device |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 15C | 2402.0 - 2480.0 | 0.002 |
| C2PC as describe in this filling. Output power is conducted. |
EAS Grant - Application XMouVUDe+y8Yf3soVK42Ww==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
St. Jude Medical 15900 Valley View Court Sylmar, CA 91342 United States |
Date of Grant: 08/01/2024 Application Dated: 08/01/2024 |
| Attention: Jennifer Wong , Director, Regulatory Affairs |
| 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: | RIAICDRFNGQ |
| Name of Grantee: | St. Jude Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | Implantable Cardioverter Defibrillator Device |
| Modular Type: | Does not apply |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 15C | 2402.0 - 2480.0 | 0.002 |
| C2PC as describe in this filling. Output power is conducted. |
| Mail To: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
TUV SUD America Inc. 401 Edgewater Place Suite #500 Wakefield, MA 01880 |
Date of Grant: 10/18/2019 Application Dated: 10/17/2019 |
| St. Jude Medical |
| 15900 Valley View Court |
| Sylmar, CA 91342 |
| Attention: Jennifer Wong , Director, Regulatory Affairs |
| 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: | RIAICDRFNGQ |
| Name of Grantee: | St. Jude Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | Implantable Cardioverter Defibrillator Device |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 15C | 2402.0 - 2480.0 | 0.002 |
| Power listed is Conducted. |
EAS Grant - Application nAEwg/RruycIoqYDk5emMg==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
St. Jude Medical 15900 Valley View Court Sylmar, CA 91342 United States |
Date of Grant: 10/18/2019 Application Dated: 10/17/2019 |
| Attention: Jennifer Wong , Director, Regulatory Affairs |
| 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: | RIAICDRFNGQ |
| Name of Grantee: | St. Jude Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | Implantable Cardioverter Defibrillator Device |
| Modular Type: | Does not apply |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 15C | 2402.0 - 2480.0 | 0.002 |
| Power listed is Conducted. |
| Mail To: | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| TCB | GRANT OF EQUIPMENT AUTHORIZATION |
TCB |
| Certification | ||
| Issued Under the Authority of the | ||
| Federal Communications Commission | ||
| By: |
|
TUV SUD America Inc. 401 Edgewater Place Suite #500 Wakefield, MA 01880 |
Date of Grant: 07/27/2023 Application Dated: 07/14/2023 |
| St. Jude Medical |
| 15900 Valley View Court |
| Sylmar, CA 91342 |
| Attention: Jennifer Wong , Director, Regulatory Affairs |
| 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: | RIAICDRFNGQ |
| Name of Grantee: | St. Jude Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | Implantable Cardioverter Defibrillator Device |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 15C | 2402.0 - 2480.0 | 0.002 |
| C2PC as described in this filling. Output power is conducted. |
EAS Grant - Application mWEBVBkUk+XKSrkzdbxOcQ==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
St. Jude Medical 15900 Valley View Court Sylmar, CA 91342 United States |
Date of Grant: 07/27/2023 Application Dated: 07/14/2023 |
| Attention: Jennifer Wong , Director, Regulatory Affairs |
| 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: | RIAICDRFNGQ |
| Name of Grantee: | St. Jude Medical |
| Equipment Class: | Digital Transmission System |
| Notes: | Implantable Cardioverter Defibrillator Device |
| Modular Type: | Does not apply |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| 15C | 2402.0 - 2480.0 | 0.002 |
| C2PC as described in this filling. Output power is conducted. |
| Mail To: |