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FDA 510(k)

FINALLY FREE

K-Number: K972695 · 1997-10-22

ApplicantMehl/Group Marketing
Decision Date1997-10-22
Product CodeKCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FINALLY FREE is the device name listed in this FDA 510(k) record. The listed applicant is Mehl/Group Marketing. It received FDA 510(k) clearance on 1997-10-22 under 510(k) number K972695. 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 FINALLY FREE?

FINALLY FREE is a medical device that received FDA 510(k) clearance on 1997-10-22. The listed applicant is Mehl/Group Marketing. The 510(k) number is K972695.

When did FINALLY FREE receive FDA 510(k) clearance?

FINALLY FREE received FDA 510(k) clearance on 1997-10-22, under 510(k) number K972695.

Who is the listed applicant for FINALLY FREE?

The FDA 510(k) record lists Mehl/Group Marketing as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FINALLY FREE?

The FDA product code for FINALLY FREE 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.K973174SONIQUE HAIR REMOVERGlobal TV Concepts, Ltd.K973179FEMINIQUE SONIC HAIR REMOVERGlobal TV Concepts, Ltd.K970338TWEEZER-TYPE EPILATORIgia Direct, Inc.K935706EPI 2Universal H.R. System, 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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