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

PORTABLE PULSE GALVANIC STIMULATOR

K Number: K791087 · Decision Oct 12, 1979
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
14
Review Days
122

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Basic Information

Device Name
PORTABLE PULSE GALVANIC STIMULATOR
K Number
K791087
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Staodynamics, Inc.
Date Received
June 12, 1979
Decision Date
October 12, 1979
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 Staodynamics, Inc.

K Number Device Name
K852298 TENS-AID STERILE ELECTRODES FOR POST-OP TENS
K843964 TENS-AID PREMIUM ELECTRODES
K832988 STAODYN EMS/PLUS
K813283 10D (TENS DEVICE)
K813098 TENS DEVICE
K811345 INSIGHT
K792529 POINT LOCATOR STIMULATOR
K792501 PLS MINI
K800068 ELECTRICAL MUSCLE STIMULATOR (EMS)
K792502 TENS 4100
Search all 14 clearances from Staodynamics, Inc. →