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FDA 510(k)

NEUROGAR IV-EXTERNAL NEURO-MUSCLE STIM.

K-Number: K801577 · 1980-08-27

ApplicantInter Med Industries, Inc.
Decision Date1980-08-27
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NEUROGAR IV-EXTERNAL NEURO-MUSCLE STIM. 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 1980-08-27 under 510(k) number K801577. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROGAR IV-EXTERNAL NEURO-MUSCLE STIM.?

NEUROGAR IV-EXTERNAL NEURO-MUSCLE STIM. is a medical device that received FDA 510(k) clearance on 1980-08-27. The listed applicant is Inter Med Industries, Inc.. The 510(k) number is K801577.

When did NEUROGAR IV-EXTERNAL NEURO-MUSCLE STIM. receive FDA 510(k) clearance?

NEUROGAR IV-EXTERNAL NEURO-MUSCLE STIM. received FDA 510(k) clearance on 1980-08-27, under 510(k) number K801577.

Who is the listed applicant for NEUROGAR IV-EXTERNAL NEURO-MUSCLE STIM.?

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 IV-EXTERNAL NEURO-MUSCLE STIM.?

The FDA product code for NEUROGAR IV-EXTERNAL NEURO-MUSCLE STIM. is IPF.

Related Clinical Trials

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.

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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.

K812036NEUROGAR IIIK801576NEUROGAR III-TRANSCUT. ELEC. NERVE STIM

Related Devices (Code: IPF)

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.

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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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