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

MAXICEPTOR

K Number: K780632 · Decision Aug 14, 1978
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
4
Applicant Total
12
Review Days
119

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Basic Information

Device Name
MAXICEPTOR
K Number
K780632
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.1850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Med General
Date Received
April 17, 1978
Decision Date
August 14, 1978
Product Code
ISB
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
ISB Stimulator, Muscle, Diagnostic

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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
K780698 STIMULATORS, NERVE, ELECTRICAL
K780117 CARDIOMETER
K771701 VESSEL-CLUDE
K771702 VESSEL-STABILIZER
Search all 12 clearances from Med General →