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FDA 510(k)

AHRS EPILATOR 629

K-Number: K892514 · 1990-08-14

ApplicantAmerican Hair Removal System Co.
Decision Date1990-08-14
Product CodeKCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AHRS EPILATOR 629 is the device name listed in this FDA 510(k) record. The listed applicant is American Hair Removal System Co.. It received FDA 510(k) clearance on 1990-08-14 under 510(k) number K892514. 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 AHRS EPILATOR 629?

AHRS EPILATOR 629 is a medical device that received FDA 510(k) clearance on 1990-08-14. The listed applicant is American Hair Removal System Co.. The 510(k) number is K892514.

When did AHRS EPILATOR 629 receive FDA 510(k) clearance?

AHRS EPILATOR 629 received FDA 510(k) clearance on 1990-08-14, under 510(k) number K892514.

Who is the listed applicant for AHRS EPILATOR 629?

The FDA 510(k) record lists American Hair Removal System Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AHRS EPILATOR 629?

The FDA product code for AHRS EPILATOR 629 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.

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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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