LF5B35200

FCC ID

Equipment:

Medtronic, Inc. B35200

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

Application
Frequency Range
Final Action Date
Granted
vFTcw9HPHDEVNZyFp0SDCw==
402.0-405.0
2022-01-14
APPROVED
File NameDocument TypeDateDirect
Labeling AttestationAttestation Statements 2022-01-14 00:00:00 pdf
family model declaration letterAttestation Statements 2022-01-14 00:00:00 pdf
Test ReportTest Report 2022-01-14 00:00:00 pdf
RF Exposure InfoRF Exposure Info 2022-01-14 00:00:00 pdf
ID Label/Location InfoID Label/Location Info 2022-01-14 00:00:00 pdf
FCC Confidentiality Request LetterCover Letter(s) 2022-01-14 00:00:00 pdf
FCC Agent Authorization LetterCover Letter(s) 2022-01-14 00:00:00 pdf
Block DiagramBlock Diagram N/A
External PhotosExternal Photos 2022-07-12 00:00:00 N/A
Internal PhotosInternal Photos N/A
Operational DescriptionOperational Description N/A
Tune Up InfoParts List/Tune Up Info N/A
SchematicsSchematics N/A
Test Setup PhotosTest Setup Photos 2022-07-12 00:00:00 N/A
Users ManualUsers Manual 2022-07-12 00:00:00 N/A

Application Details:

EquipmentIntellis TM Rechargeable neurostimulator
FRN0008250839
Grantee CodeLF5
Product CodeB35200
Applicant BusinessMedtronic, Inc.
Business Address8200 Coral Sea Street NE , Mounds View,Minnesota United States 55112
TCB ScopeB2: General Mobile Radio And Broadcast Services equipment in the following 47 CFR Parts 22 (non-cellular) 73, 74, 90, 95, 97, & 101 (all below 3 GHz)
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 ByGuillaume Girard – EMC and RF Regulatory Compliance Technical Fellow

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