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

CEPTOR HESIVE

K Number: K790269 · Decision Feb 26, 1979
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
12
Review Days
21

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Basic Information

Device Name
CEPTOR HESIVE
K Number
K790269
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Med General
Date Received
February 5, 1979
Decision Date
February 26, 1979
Product Code
GXY
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
GXY Electrode, Cutaneous

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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
K782006 MEDGENERAL SINGLE-USE BULLDOG
K781239 MYO-STIM
K780632 MAXICEPTOR
K780698 STIMULATORS, NERVE, ELECTRICAL
K780117 CARDIOMETER
K771701 VESSEL-CLUDE
K771702 VESSEL-STABILIZER
Search all 12 clearances from Med General →