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FDA 510(k)

E.W.L. P-TENS/H-WAVE FOR GENERAL DENTISTRY

K-Number: K873604 · 1988-04-12

Decision Date1988-04-12
Product CodeLWM
DecisionSubstantially Equivalent

Device Summary

E.W.L. P-TENS/H-WAVE FOR GENERAL DENTISTRY 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 1988-04-12 under 510(k) number K873604. The device is classified under product code LWM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E.W.L. P-TENS/H-WAVE FOR GENERAL DENTISTRY?

E.W.L. P-TENS/H-WAVE FOR GENERAL DENTISTRY is a medical device that received FDA 510(k) clearance on 1988-04-12. The listed applicant is Electronic Waveform Laboratory, Inc.. The 510(k) number is K873604.

When did E.W.L. P-TENS/H-WAVE FOR GENERAL DENTISTRY receive FDA 510(k) clearance?

E.W.L. P-TENS/H-WAVE FOR GENERAL DENTISTRY received FDA 510(k) clearance on 1988-04-12, under 510(k) number K873604.

Who is the listed applicant for E.W.L. P-TENS/H-WAVE FOR GENERAL DENTISTRY?

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 E.W.L. P-TENS/H-WAVE FOR GENERAL DENTISTRY?

The FDA product code for E.W.L. P-TENS/H-WAVE FOR GENERAL DENTISTRY is LWM.

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: LWM)

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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