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FDA 510(k)

H WAVE MUSCLE STIMULATOR

K-Number: K915230 · 1992-05-08

Decision Date1992-05-08
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

H WAVE MUSCLE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Electronic Waveform Laboratory, Inc.. It received FDA 510(k) clearance on 1992-05-08 under 510(k) number K915230. 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 H WAVE MUSCLE STIMULATOR?

H WAVE MUSCLE STIMULATOR is a medical device that received FDA 510(k) clearance on 1992-05-08. The listed applicant is Electronic Waveform Laboratory, Inc.. The 510(k) number is K915230.

When did H WAVE MUSCLE STIMULATOR receive FDA 510(k) clearance?

H WAVE MUSCLE STIMULATOR received FDA 510(k) clearance on 1992-05-08, under 510(k) number K915230.

Who is the listed applicant for H WAVE MUSCLE STIMULATOR?

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

What is the FDA product code for H WAVE MUSCLE STIMULATOR?

The FDA product code for H WAVE MUSCLE STIMULATOR 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.

Other records listing Electronic Waveform Laboratory, 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.

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.

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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