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

INSIGHT

K Number: K811345 · Decision Jul 10, 1981
Classifications
1
FEI Numbers
179
Registration Numbers
179
Same Product Code
601
Applicant Total
14
Review Days
59

Basic Information

Device Name
INSIGHT
K Number
K811345
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
STAODYNAMICS, INC.
Date Received
May 12, 1981
Decision Date
July 10, 1981
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

Other 510(k) clearances with the same product code (GZJ), ordered by most recent decision date.

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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
K792529 POINT LOCATOR STIMULATOR
K792501 PLS MINI
K800068 ELECTRICAL MUSCLE STIMULATOR (EMS)
K792502 TENS 4100
K792474 TENS 4500
Search all 14 clearances from STAODYNAMICS, INC. →