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FDA 510(k)

KENATRON EPILATOR

K-Number: K761049 · 1977-01-05

ApplicantEpilator Corp.
Decision Date1977-01-05
Product CodeKCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KENATRON EPILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Epilator Corp.. It received FDA 510(k) clearance on 1977-01-05 under 510(k) number K761049. 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 KENATRON EPILATOR?

KENATRON EPILATOR is a medical device that received FDA 510(k) clearance on 1977-01-05. The listed applicant is Epilator Corp.. The 510(k) number is K761049.

When did KENATRON EPILATOR receive FDA 510(k) clearance?

KENATRON EPILATOR received FDA 510(k) clearance on 1977-01-05, under 510(k) number K761049.

Who is the listed applicant for KENATRON EPILATOR?

The FDA 510(k) record lists Epilator Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KENATRON EPILATOR?

The FDA product code for KENATRON EPILATOR is KCX.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.K973174SONIQUE HAIR REMOVERGlobal TV Concepts, Ltd.K973179FEMINIQUE SONIC 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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