ELECTRO-BLEND EPILATOR, MODEL UC-3— 510(k) K904015

Name: FDA 510(k) clearance K904015
Creator: U.S. Food and Drug Administration
Published: 1990-10-04

Substantially Equivalent

A.R. Hinkel Co., Inc.

FDA 510(k) clearance K904015 for ELECTRO-BLEND EPILATOR, MODEL UC-3, Substantially Equivalent on 1990-10-04. Applicant: A.R. Hinkel Co., Inc.. Device class: 1.

Clearance details

Applicant: A.R. Hinkel Co., Inc.
Product code: Code KCW
Device class: Class 1
Regulation: 21 CFR 878.5350
Advisory panel: General, Plastic Surgery
Date received: 1990-08-31
Decision date: 1990-10-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Northridge, CA, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.