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FDA 510(k)

LINDSTROM CORDLESS EPILATOR

K-Number: K883429 · 1988-09-28

ApplicantA Place of Health & Beauty
Decision Date1988-09-28
Product CodeKCW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LINDSTROM CORDLESS EPILATOR is the device name listed in this FDA 510(k) record. The listed applicant is A Place of Health & Beauty. It received FDA 510(k) clearance on 1988-09-28 under 510(k) number K883429. 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 LINDSTROM CORDLESS EPILATOR?

LINDSTROM CORDLESS EPILATOR is a medical device that received FDA 510(k) clearance on 1988-09-28. The listed applicant is A Place of Health & Beauty. The 510(k) number is K883429.

When did LINDSTROM CORDLESS EPILATOR receive FDA 510(k) clearance?

LINDSTROM CORDLESS EPILATOR received FDA 510(k) clearance on 1988-09-28, under 510(k) number K883429.

Who is the listed applicant for LINDSTROM CORDLESS EPILATOR?

The FDA 510(k) record lists A Place of Health & Beauty as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LINDSTROM CORDLESS EPILATOR?

The FDA product code for LINDSTROM CORDLESS EPILATOR 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

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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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