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FDA 510(k)

NEUROGAR III

K-Number: K812036 · 1981-08-07

ApplicantInter Med Industries, Inc.
Decision Date1981-08-07
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROGAR III is the device name listed in this FDA 510(k) record. The listed applicant is Inter Med Industries, Inc.. It received FDA 510(k) clearance on 1981-08-07 under 510(k) number K812036. 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 NEUROGAR III?

NEUROGAR III is a medical device that received FDA 510(k) clearance on 1981-08-07. The listed applicant is Inter Med Industries, Inc.. The 510(k) number is K812036.

When did NEUROGAR III receive FDA 510(k) clearance?

NEUROGAR III received FDA 510(k) clearance on 1981-08-07, under 510(k) number K812036.

Who is the listed applicant for NEUROGAR III?

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

What is the FDA product code for NEUROGAR III?

The FDA product code for NEUROGAR III is GZJ.

Related Clinical Trials

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Other records listing Inter Med Industries, 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.

K801577NEUROGAR IV-EXTERNAL NEURO-MUSCLE STIM.K801576NEUROGAR III-TRANSCUT. ELEC. NERVE STIM

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

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

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