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FDA 510(k)

ELECTRONIC DEPILATORY MODEL 303

K-Number: K770187 · 1977-02-23

ApplicantElectronic Depilatory, Inc.
Decision Date1977-02-23
Product CodeKCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC DEPILATORY MODEL 303 is the device name listed in this FDA 510(k) record. The listed applicant is Electronic Depilatory, Inc.. It received FDA 510(k) clearance on 1977-02-23 under 510(k) number K770187. 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 ELECTRONIC DEPILATORY MODEL 303?

ELECTRONIC DEPILATORY MODEL 303 is a medical device that received FDA 510(k) clearance on 1977-02-23. The listed applicant is Electronic Depilatory, Inc.. The 510(k) number is K770187.

When did ELECTRONIC DEPILATORY MODEL 303 receive FDA 510(k) clearance?

ELECTRONIC DEPILATORY MODEL 303 received FDA 510(k) clearance on 1977-02-23, under 510(k) number K770187.

Who is the listed applicant for ELECTRONIC DEPILATORY MODEL 303?

The FDA 510(k) record lists Electronic Depilatory, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRONIC DEPILATORY MODEL 303?

The FDA product code for ELECTRONIC DEPILATORY MODEL 303 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

Other records listing Electronic Depilatory, 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.

K771575ELECTRONIC EIPLATOR MODEL NO. 101K770186ELECTRONIC DEPILATORY MODEL 202

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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