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FDA 510(k)

HIGH FREQUENCY EPILATOR CB-2

K-Number: K823674 · 1983-01-14

ApplicantR. A. Fischer Co. Corp.
Decision Date1983-01-14
Product CodeKCW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HIGH FREQUENCY EPILATOR CB-2 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 1983-01-14 under 510(k) number K823674. 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 HIGH FREQUENCY EPILATOR CB-2?

HIGH FREQUENCY EPILATOR CB-2 is a medical device that received FDA 510(k) clearance on 1983-01-14. The listed applicant is R. A. Fischer Co. Corp.. The 510(k) number is K823674.

When did HIGH FREQUENCY EPILATOR CB-2 receive FDA 510(k) clearance?

HIGH FREQUENCY EPILATOR CB-2 received FDA 510(k) clearance on 1983-01-14, under 510(k) number K823674.

Who is the listed applicant for HIGH FREQUENCY EPILATOR CB-2?

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 HIGH FREQUENCY EPILATOR CB-2?

The FDA product code for HIGH FREQUENCY EPILATOR CB-2 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 UNITK893389MODEL SE-5 EPILATORK884079MODEL CBX EPILATORK871372CB-7 ELECTRONIC EPILATOR

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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.K943399THE SS-99InstantronK943396THE 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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