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FDA 510(k)

OMNIPROBE ELECTRICAL NERVE STIMULATOR

K-Number: K831147 · 1983-07-18

ApplicantOmni Intl., Inc.
Decision Date1983-07-18
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

OMNIPROBE ELECTRICAL NERVE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Omni Intl., Inc.. It received FDA 510(k) clearance on 1983-07-18 under 510(k) number K831147. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMNIPROBE ELECTRICAL NERVE STIMULATOR?

OMNIPROBE ELECTRICAL NERVE STIMULATOR is a medical device that received FDA 510(k) clearance on 1983-07-18. The listed applicant is Omni Intl., Inc.. The 510(k) number is K831147.

When did OMNIPROBE ELECTRICAL NERVE STIMULATOR receive FDA 510(k) clearance?

OMNIPROBE ELECTRICAL NERVE STIMULATOR received FDA 510(k) clearance on 1983-07-18, under 510(k) number K831147.

Who is the listed applicant for OMNIPROBE ELECTRICAL NERVE STIMULATOR?

The FDA 510(k) record lists Omni Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OMNIPROBE ELECTRICAL NERVE STIMULATOR?

The FDA product code for OMNIPROBE ELECTRICAL NERVE STIMULATOR is GZJ.

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Other records listing Omni Intl., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K984066OMNIGRIP, LATEX SURGICAL GLOVE, POWDER-FREE WITH PROTEIN LABELING CLAIMK984064OMNIGRIP, LATEX SURGICAL GLOVE, POWDER FREEK853255OMNIMED I.V. SOLUTION ADMIN. SETK851938OMNIMED SURGICAL GOWNK851654OMNIMED CLAMPK851734OMNIMED SUPERIOR TRANSDUCER PROTECTOR

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Related Devices (Code: GZJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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