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

NEUROMUSCULAR STIMULATOR

K Number: K932611 · Decision Jan 31, 1994
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
8
Review Days
248

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Basic Information

Device Name
NEUROMUSCULAR STIMULATOR
K Number
K932611
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Myo/Kinetic Systems, Inc.
Date Received
May 28, 1993
Decision Date
January 31, 1994
Product Code
GZJ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

Similar 510(k) Clearances

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Other Clearances by Myo/Kinetic Systems, Inc.

K Number Device Name
K945937 TE-800 PELVIC FLOOR EXERCISER
K945292 TS-700P CONTROL XP ELECTRICAL STIMULATOR
K944972 URO-GRAM CYSTOMRTROGRAM WITH UROFLOWMETRY
K936041 UROGRAM CYSTOMETROGRAM
K932764 THERAPEUTIC STIMULATOR 300(TS-300) & 300P(TS-300P)
K932399 THERAPEUTIC STIM 200 (TS-200)/200P (TS-200P)
K914904 THERAPEUTIC STIMULATOR 2100 (TS-2100)