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

MYO-STIM

K Number: K781239 · Decision Nov 3, 1978
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
12
Review Days
106

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Basic Information

Device Name
MYO-STIM
K Number
K781239
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Med General
Date Received
July 20, 1978
Decision Date
November 3, 1978
Product Code
IPF
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
IPF Stimulator, Muscle, Powered

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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
K780632 MAXICEPTOR
K780698 STIMULATORS, NERVE, ELECTRICAL
K780117 CARDIOMETER
K771701 VESSEL-CLUDE
K771702 VESSEL-STABILIZER
Search all 12 clearances from Med General →