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FDA 510(k)

ELECTRO-BLEND EPILATOR, MODEL UC-3

K-Number: K904015 · 1990-10-04

Decision Date1990-10-04
Product CodeKCW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTRO-BLEND EPILATOR, MODEL UC-3 is the device name listed in this FDA 510(k) record. The listed applicant is A.R. Hinkel Co., Inc.. It received FDA 510(k) clearance on 1990-10-04 under 510(k) number K904015. 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 ELECTRO-BLEND EPILATOR, MODEL UC-3?

ELECTRO-BLEND EPILATOR, MODEL UC-3 is a medical device that received FDA 510(k) clearance on 1990-10-04. The listed applicant is A.R. Hinkel Co., Inc.. The 510(k) number is K904015.

When did ELECTRO-BLEND EPILATOR, MODEL UC-3 receive FDA 510(k) clearance?

ELECTRO-BLEND EPILATOR, MODEL UC-3 received FDA 510(k) clearance on 1990-10-04, under 510(k) number K904015.

Who is the listed applicant for ELECTRO-BLEND EPILATOR, MODEL UC-3?

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

What is the FDA product code for ELECTRO-BLEND EPILATOR, MODEL UC-3?

The FDA product code for ELECTRO-BLEND EPILATOR, MODEL UC-3 is KCW.

Related Clinical Trials

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.

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.

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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