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

NEUROGAR IV-EXTERNAL NEURO-MUSCLE STIM.

K Number: K801577 · Decision Aug 27, 1980
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
3
Review Days
49

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Basic Information

Device Name
NEUROGAR IV-EXTERNAL NEURO-MUSCLE STIM.
K Number
K801577
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Inter Med Industries, Inc.
Date Received
July 9, 1980
Decision Date
August 27, 1980
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 Inter Med Industries, Inc.

K Number Device Name
K812036 NEUROGAR III
K801576 NEUROGAR III-TRANSCUT. ELEC. NERVE STIM