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FDA 510(k)

FEMINIQUE SONIC HAIR REMOVER

K-Number: K973179 · 1997-10-30

ApplicantGlobal TV Concepts, Ltd.
Decision Date1997-10-30
Product CodeKCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FEMINIQUE SONIC HAIR REMOVER is the device name listed in this FDA 510(k) record. The listed applicant is Global TV Concepts, Ltd.. It received FDA 510(k) clearance on 1997-10-30 under 510(k) number K973179. 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 FEMINIQUE SONIC HAIR REMOVER?

FEMINIQUE SONIC HAIR REMOVER is a medical device that received FDA 510(k) clearance on 1997-10-30. The listed applicant is Global TV Concepts, Ltd.. The 510(k) number is K973179.

When did FEMINIQUE SONIC HAIR REMOVER receive FDA 510(k) clearance?

FEMINIQUE SONIC HAIR REMOVER received FDA 510(k) clearance on 1997-10-30, under 510(k) number K973179.

Who is the listed applicant for FEMINIQUE SONIC HAIR REMOVER?

The FDA 510(k) record lists Global TV Concepts, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FEMINIQUE SONIC HAIR REMOVER?

The FDA product code for FEMINIQUE SONIC HAIR REMOVER 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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Other records listing Global TV Concepts, Ltd. 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.

K013707SOFTIQUE, MODEL GI 11001K973174SONIQUE HAIR REMOVER

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.K972695FINALLY FREEMehl/Group MarketingK970338TWEEZER-TYPE EPILATORIgia Direct, Inc.K935706EPI 2Universal H.R. System, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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