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FDA 510(k)

COMPU-BLEND EPILATOR

K-Number: K954031 · 1996-01-05

ApplicantR. A. Fischer Co. Corp.
Decision Date1996-01-05
Product CodeKCW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COMPU-BLEND EPILATOR is the device name listed in this FDA 510(k) record. The listed applicant is R. A. Fischer Co. Corp.. It received FDA 510(k) clearance on 1996-01-05 under 510(k) number K954031. 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 COMPU-BLEND EPILATOR?

COMPU-BLEND EPILATOR is a medical device that received FDA 510(k) clearance on 1996-01-05. The listed applicant is R. A. Fischer Co. Corp.. The 510(k) number is K954031.

When did COMPU-BLEND EPILATOR receive FDA 510(k) clearance?

COMPU-BLEND EPILATOR received FDA 510(k) clearance on 1996-01-05, under 510(k) number K954031.

Who is the listed applicant for COMPU-BLEND EPILATOR?

The FDA 510(k) record lists R. A. Fischer Co. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPU-BLEND EPILATOR?

The FDA product code for COMPU-BLEND EPILATOR is KCW.

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Other records listing R. A. Fischer Co. Corp. 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.

K964208MD-1A GALVANIC UNITK895365MD-2 IONTOPHORESIS UNITK893389MODEL SE-5 EPILATORK884079MODEL CBX EPILATORK871372CB-7 ELECTRONIC EPILATORK852534ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9

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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.

K952611STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATIONSterex Electrolysis Intl., Ltd.K943928APILUS ELECTROPILDectro Intl., Inc.K945192HAIR REMOVAL SYSTEML.P. Systems Corp.K943398THE BLENDTONE ROYALEInstantronK943396THE ELITE SPECTRUMInstantronK943399THE SS-99Instantron

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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