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FDA 510(k)

D'PLUME XXII PHOTOCOAGULATOR (EPILATION MACHINE)

K-Number: K895687 · 1990-08-09

ApplicantCarol Block, Ltd.
Decision Date1990-08-09
Product CodeKCW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

D'PLUME XXII PHOTOCOAGULATOR (EPILATION MACHINE) is the device name listed in this FDA 510(k) record. The listed applicant is Carol Block, Ltd.. It received FDA 510(k) clearance on 1990-08-09 under 510(k) number K895687. The device is classified under product code KCW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the D'PLUME XXII PHOTOCOAGULATOR (EPILATION MACHINE)?

D'PLUME XXII PHOTOCOAGULATOR (EPILATION MACHINE) is a medical device that received FDA 510(k) clearance on 1990-08-09. The listed applicant is Carol Block, Ltd.. The 510(k) number is K895687.

When did D'PLUME XXII PHOTOCOAGULATOR (EPILATION MACHINE) receive FDA 510(k) clearance?

D'PLUME XXII PHOTOCOAGULATOR (EPILATION MACHINE) received FDA 510(k) clearance on 1990-08-09, under 510(k) number K895687.

Who is the listed applicant for D'PLUME XXII PHOTOCOAGULATOR (EPILATION MACHINE)?

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

What is the FDA product code for D'PLUME XXII PHOTOCOAGULATOR (EPILATION MACHINE)?

The FDA product code for D'PLUME XXII PHOTOCOAGULATOR (EPILATION MACHINE) is KCW.

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Related Devices (Code: KCW)

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.

K954031COMPU-BLEND EPILATORR. A. Fischer Co. Corp.K952611STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATIONSterex Electrolysis Intl., Ltd.K945192HAIR REMOVAL SYSTEML.P. Systems Corp.K943928APILUS ELECTROPILDectro Intl., Inc.K943398THE BLENDTONE ROYALEInstantronK943396THE ELITE SPECTRUMInstantron

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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