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FDA 510(k)

DEPILATOR, DERMA-I & DERMA-II

K-Number: K770791 · 1981-01-26

ApplicantElectro-Kinetic Eng/Mfg
Decision Date1981-01-26
Product CodeKCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEPILATOR, DERMA-I & DERMA-II is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Kinetic Eng/Mfg. It received FDA 510(k) clearance on 1981-01-26 under 510(k) number K770791. The device is classified under product code KCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEPILATOR, DERMA-I & DERMA-II?

DEPILATOR, DERMA-I & DERMA-II is a medical device that received FDA 510(k) clearance on 1981-01-26. The listed applicant is Electro-Kinetic Eng/Mfg. The 510(k) number is K770791.

When did DEPILATOR, DERMA-I & DERMA-II receive FDA 510(k) clearance?

DEPILATOR, DERMA-I & DERMA-II received FDA 510(k) clearance on 1981-01-26, under 510(k) number K770791.

Who is the listed applicant for DEPILATOR, DERMA-I & DERMA-II?

The FDA 510(k) record lists Electro-Kinetic Eng/Mfg as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEPILATOR, DERMA-I & DERMA-II?

The FDA product code for DEPILATOR, DERMA-I & DERMA-II is KCX.

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Related Devices (Code: KCX)

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.

K973773DAPELLE HAIR REMOVERWellquest Intl., Inc.K973340TWEEZER-TYPE EPILATORMobit, Inc.K973179FEMINIQUE SONIC HAIR REMOVERGlobal TV Concepts, Ltd.K973174SONIQUE HAIR REMOVERGlobal TV Concepts, Ltd.K972695FINALLY FREEMehl/Group MarketingK970338TWEEZER-TYPE EPILATORIgia Direct, Inc.

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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