H WAVE MUSCLE STIMULATOR
K-Number: K915230 · 1992-05-08
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Device Summary
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
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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