FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

STIMULATORS, NERVE, ELECTRICAL

K Number: K780698 · Decision May 12, 1978
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
12
Review Days
16

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Basic Information

Device Name
STIMULATORS, NERVE, ELECTRICAL
K Number
K780698
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Med General
Date Received
April 26, 1978
Decision Date
May 12, 1978
Product Code
GZJ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

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Other Clearances by Med General

K Number Device Name
K791097 CEPTORTRODE WITH CEPTOR HESIVE
K791098 SINGLE-USE MINI-BULLDOG
K790763 MAXI-VAC TM
K790269 CEPTOR HESIVE
K782006 MEDGENERAL SINGLE-USE BULLDOG
K781239 MYO-STIM
K780632 MAXICEPTOR
K780117 CARDIOMETER
K771701 VESSEL-CLUDE
K771702 VESSEL-STABILIZER
Search all 12 clearances from Med General →