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

OMNIPROBE ELECTRICAL NERVE STIMULATOR

K Number: K831147 · Decision Jul 18, 1983
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
12
Review Days
101

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Basic Information

Device Name
OMNIPROBE ELECTRICAL NERVE STIMULATOR
K Number
K831147
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Omni Intl., Inc.
Date Received
April 8, 1983
Decision Date
July 18, 1983
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 Omni Intl., Inc.

K Number Device Name
K984066 OMNIGRIP, LATEX SURGICAL GLOVE, POWDER-FREE WITH PROTEIN LABELING CLAIM
K984064 OMNIGRIP, LATEX SURGICAL GLOVE, POWDER FREE
K853255 OMNIMED I.V. SOLUTION ADMIN. SET
K851938 OMNIMED SURGICAL GOWN
K851654 OMNIMED CLAMP
K851734 OMNIMED SUPERIOR TRANSDUCER PROTECTOR
K850706 F-SERIES IMPLANT
K850112 OMNIMED IV SOLUTION ADMINISTRATION SET
K850066 OMNIMED NASAL OXYGEN CANNULA
K821523 OMNI TENS
Search all 12 clearances from Omni Intl., Inc. →