LF597800

FCC ID

Equipment:

Medtronic, Inc. 97800

8200 Coral Sea Street NE, Mounds View, MN 55112 United States

Application
Frequency Range
Final Action Date
Granted
CL0SX1jwyt1+I44lHhzzew==
0.175-0.175
2022-09-09
APPROVED
File NameDocument TypeDateDirect
Sample NDACover Letter(s) 2022-09-09 00:00:00 pdf
Test Setup PhotosTest Setup Photos 2022-09-09 00:00:00 pdf
User ManualUsers Manual 2022-09-09 00:00:00 pdf
Product Certification Representative Auth LetterCover Letter(s) 2022-09-09 00:00:00 pdf
Product LabelID Label/Location Info 2022-09-09 00:00:00 pdf
External PhotosExternal Photos 2022-09-09 00:00:00 pdf
RF Exposure ReportRF Exposure Info 2022-09-09 00:00:00 pdf
Test ReportTest Report 2022-09-09 00:00:00 pdf
Confidentiality Request LetterCover Letter(s) 2022-09-09 00:00:00 pdf
Manual InsertUsers Manual 2022-09-09 00:00:00 pdf
Block DiagramBlock Diagram N/A
Internal PhotosInternal Photos N/A
Internal Assembly PhotoInternal Photos N/A
Operational DescriptionOperational Description N/A
SchematicsSchematics N/A

Application Details:

EquipmentUltra Low Power Active Medical Implant (ULP-AMI)
FRN0008250839
Grantee CodeLF5
Product Code97800
Applicant BusinessMedtronic, Inc.
Business Address8200 Coral Sea Street NE , Mounds View,Minnesota United States 55112
TCB ScopeA1: Low Power Transmitters below 1 GHz (except Spread Spectrum), Unintentional Radiators, EAS (Part 11) & Consumer ISM devices
TCB Email[email protected]
ApplicantGuillaume Girard – Sr. RF Regulatory Program Manager
Applicant Phone
Applicant Fax651-367-0603
Applicant Email[email protected]
Applicant MailStop
Test FirmBureau Veritas Consumer Products Services, Inc.
Test Firm ContactSarb Shelopal
Test Firm Phone
Test Firm Fax
Test Firm Email[email protected]
Certified ByGirard Guillaume – Senior Compliance manager

© 2024 FCC.report
This site is not affiliated with or endorsed by the FCC