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FDA 510(k)

MICROPROCESSOR CONTR/MULTI-NEEDLE, GALVAN EPILATOR

K-Number: K864289 · 1986-12-01

ApplicantAlexander Thomas, Inc.
Decision Date1986-12-01
Product CodeKCW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICROPROCESSOR CONTR/MULTI-NEEDLE, GALVAN EPILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Alexander Thomas, Inc.. It received FDA 510(k) clearance on 1986-12-01 under 510(k) number K864289. 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 MICROPROCESSOR CONTR/MULTI-NEEDLE, GALVAN EPILATOR?

MICROPROCESSOR CONTR/MULTI-NEEDLE, GALVAN EPILATOR is a medical device that received FDA 510(k) clearance on 1986-12-01. The listed applicant is Alexander Thomas, Inc.. The 510(k) number is K864289.

When did MICROPROCESSOR CONTR/MULTI-NEEDLE, GALVAN EPILATOR receive FDA 510(k) clearance?

MICROPROCESSOR CONTR/MULTI-NEEDLE, GALVAN EPILATOR received FDA 510(k) clearance on 1986-12-01, under 510(k) number K864289.

Who is the listed applicant for MICROPROCESSOR CONTR/MULTI-NEEDLE, GALVAN EPILATOR?

The FDA 510(k) record lists Alexander Thomas, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROPROCESSOR CONTR/MULTI-NEEDLE, GALVAN EPILATOR?

The FDA product code for MICROPROCESSOR CONTR/MULTI-NEEDLE, GALVAN 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 ROYALEInstantronK943399THE SS-99Instantron

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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