FCC ID LF597715
Implantable Neurostimulator
by Medtronic, Inc.
Grantee Code: LF5 Product Code: 97715
Latest application date: 2017-05-16
Device Images
FCC ID Device Details
| FCC ID | LF597715 |
|---|---|
| Mirrors | fcc.id | gov | fccid.ai |
| Grantee Code | LF5 |
| Product Code | 97715 |
| Applicant Business | Medtronic, Inc. 🇺🇸 |
| Related Domains |  medtronic.com |
| Equipment Class | Implantable Neurostimulator |
| Test Firm | Bureau Veritas Consumer Products Services, Inc. |
Operating Frequencies
| Frequency Range | Application Purpose | Final Action Date |
|---|---|---|
| 402-405 MHz | Original Equipment | 2017-05-16 |
| 402-405 MHz | Original Equipment | 2014-11-25 |
Exhibits
| Document | Type | Available | File |
|---|---|---|---|
| User Manual | Users Manual | 2017-05-16 | PDF 574.3 KB |
| FCC ID manual and sterile pack info Metadata only | ID Label/Location Info | PDF 981.9 KB | |
| User Manual Part 2 Metadata only | Users Manual | PDF 5.4 MB | |
| User manual Part 1 Metadata only | Users Manual | PDF 4.7 MB | |
| Users manual Part 3 Metadata only | Users Manual | PDF 3.5 MB | |
| users manual part 4 Metadata only | Users Manual | PDF 5.2 MB | |
| users manual part 5 Metadata only | Users Manual | PDF 5.4 MB | |
| users manual part 6 Metadata only | Users Manual | PDF 4.8 MB | |
| users manual part 7 Metadata only | Users Manual | PDF 5.6 MB | |
| Internal Photos | Internal Photos | 2017-05-16 | PDF 946.9 KB |
| External Photos | External Photos | 2017-05-16 | PDF 253.1 KB |
| External Photos Metadata only | External Photos | PDF 943.9 KB | |
| FCC ID Alternative Label | ID Label/Location Info | 2017-05-16 | PDF 149.2 KB |
| Test Setup Photos | Test Setup Photos | 2017-05-16 | PDF 277.4 KB |
| Test site photos Metadata only | Test Setup Photos | PDF 200.7 KB | |
| Part 95I Test Report Metadata only | Test Report | 2017-05-16 | PDF 2.6 MB |
| TNT Test Report | Test Report | 2017-05-16 | PDF 2.6 MB |
| Revised test report Metadata only | Test Report | PDF 521.6 KB | |
| Test report Metadata only | Test Report | PDF 1,000.9 KB | |
| Alternative Labeling Attestation | Attestation Statements | 2017-05-16 | PDF 30 KB |
| Confidentiality Request Letter | Cover Letter(s) | 2017-05-16 | PDF 156.1 KB |
| Family Model Letter | Cover Letter(s) | 2017-05-16 | PDF 19.5 KB |
| PoA | Cover Letter(s) | 2017-05-16 | PDF 1.7 MB |
| Product Certification Representative Auth Letter | Cover Letter(s) | 2017-05-16 | PDF 42.8 KB |
| COVER LETTER | Cover Letter(s) | PDF 27.3 KB | |
| Cross reference between Part 2 and Part 95 | Cover Letter(s) | PDF 134.1 KB | |
| Long term short term confidentiality request | Cover Letter(s) | PDF 272.5 KB | |
| Responce to questions from reviewer | Cover Letter(s) | PDF 154.1 KB | |
| SAR Exclusion | RF Exposure Info | 2017-05-16 | PDF 83.3 KB |
| RF Exposure report Metadata only | RF Exposure Info | PDF 2.2 MB | |
| Internal Photos Metadata only | Internal Photos | PDF 81.9 KB | |
| Block Diagram Metadata only | Block Diagram | PDF 149.5 KB | |
| Block Diagram Metadata only | Block Diagram | PDF 319.3 KB | |
| Schematics Metadata only | Schematics | PDF 1.3 MB | |
| Schematics Metadata only | Schematics | PDF 1.1 MB | |
| Operational Description Metadata only | Operational Description | PDF 161.1 KB | |
| Theory of Operation Metadata only | Operational Description | PDF 37.1 KB | |
| Parts List Metadata only | Parts List/Tune Up Info | PDF 374.2 KB | |
| Parts List Metadata only | Parts List/Tune Up Info | PDF 804.4 KB |
Application Information
| Application ID | qWmHMQpZY4q9g/AB4tOhMQ== |
|---|---|
| Final Action Date | 2017-05-16 |
| Application Purpose | Original Equipment |
| Applicant FRN | 0008250839 |
| Model | 97715 |
| Frequency Range | 402-405 MHz |
| Equipment Class | TNT - Licensed Non-Broadcast Transmitter Worn on Body |
| Device Description | Implantable Neurostimulator |
| Responsible Party | Guillaume Girard, Sr. RF Regulatory Program Manager, Guillaume.Girard@medtronic.com , 763-526-0652 |
| Test Firm | Sarb Shelopal, Bureau Veritas Consumer Products Services, Inc., Sarbjit.Shelopal@bureauveritas.com  , +1 925 963 4420 |
| TCB Email | tcb@siemic.com  |
| TCB Scope | B1: Commercial mobile radio services equipment in the following 47 CFR Parts 20, 22 (cellular), 24,25 (below 3 GHz) & 27 |
| Short-Term Confidentiality | No |
| Long-Term Confidentiality | Yes |
| 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 | Output power is EIRP. |
Applications
| Application ID | Date | Purpose |
|---|---|---|
| qWmHMQpZY4q9g/AB4tOhMQ== | 2017-05-16 | Original Equipment |
| Bjh68Wx9BHr/bn0dhwum2Q== | 2014-11-25 | Original Equipment |
Equipment Authorization
Grants
TCB Grant - Application qWmHMQpZY4q9g/AB4tOhMQ==
| 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: 05/16/2017 Application Dated: 05/16/2017 |
| Medtronic, Inc. |
| 8200 Coral Sea Street NE |
| Mounds View, MN 55112 |
| Attention: Guillaume Girard , Sr. RF Regulatory Program Manager |
| 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: | LF597715 |
| Name of Grantee: | Medtronic, Inc. |
| Equipment Class: | Licensed Non-Broadcast Transmitter Worn on Body |
| Notes: | Implantable Neurostimulator |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| IT | 95I | 402.0 - 405.0 | 0.000001 | 9.5 PM | 58K2F1D |
| Output power is EIRP. |
| IT: | Implanted Transmitter |
EAS Grant - Application qWmHMQpZY4q9g/AB4tOhMQ==
| COPY |
FEDERAL COMMUNICATIONS COMMISSION WASHINGTON, D.C. 20554 GRANT OF EQUIPMENT AUTHORIZATION |
COPY |
| Certification |
|
Medtronic, Inc. 8200 Coral Sea Street NE Mounds View, MN 55112 United States |
Date of Grant: 05/16/2017 Application Dated: 05/16/2017 |
| Attention: Guillaume Girard , Sr. RF Regulatory Program Manager |
| 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: | LF597715 |
| Name of Grantee: | Medtronic, Inc. |
| Equipment Class: | Licensed Non-Broadcast Transmitter Worn on Body |
| Notes: | Implantable Neurostimulator |
| Modular Type: | Does not apply |
| Grant Notes | FCC Rule Parts | Frequency Range (MHZ) | Output Watts | Frequency Tolerance | Emission Designator |
| IT | 95I | 402.0 - 405.0 | 0.000001 | 9.5 PM | 58K2F1D |
| Output power is EIRP. |
| IT: | Implanted Transmitter |
| Mail To: |