ELECTRO-BLEND EPILATOR, MODEL UC-3
K-Number: K904015 · 1990-10-04
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Device Summary
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
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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