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FDA 510(k)

MODEL SE-5 EPILATOR

K-Number: K893389 · 1989-06-05

ApplicantR. A. Fischer Co. Corp.
Decision Date1989-06-05
Product CodeKCW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODEL SE-5 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 1989-06-05 under 510(k) number K893389. 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 MODEL SE-5 EPILATOR?

MODEL SE-5 EPILATOR is a medical device that received FDA 510(k) clearance on 1989-06-05. The listed applicant is R. A. Fischer Co. Corp.. The 510(k) number is K893389.

When did MODEL SE-5 EPILATOR receive FDA 510(k) clearance?

MODEL SE-5 EPILATOR received FDA 510(k) clearance on 1989-06-05, under 510(k) number K893389.

Who is the listed applicant for MODEL SE-5 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 MODEL SE-5 EPILATOR?

The FDA product code for MODEL SE-5 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 UNITK954031COMPU-BLEND EPILATORK895365MD-2 IONTOPHORESIS UNITK884079MODEL 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.

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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