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

ELECTRIC MUSCLE STIMULATOR

K Number: K813533 · Decision Mar 5, 1982
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
8
Review Days
78

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Basic Information

Device Name
ELECTRIC MUSCLE STIMULATOR
K Number
K813533
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Myo-Tronics Research, Inc.
Date Received
December 17, 1981
Decision Date
March 5, 1982
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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K842223 J4 MYO-MONITOR
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K831364 TESTCORP RA
K830034 MODEL EM-2 BIOELECTRIC PROCESSOR
K810528 MODEL EM-IR
K770252 MONITOR, MYO, MODEL J3