HIGH FREQUENCY EPILATOR CB-2— 510(k) K823674

Name: FDA 510(k) clearance K823674
Creator: U.S. Food and Drug Administration
Published: 1983-01-14

Substantially Equivalent

R. A. Fischer Co. Corp.

FDA 510(k) clearance K823674 for HIGH FREQUENCY EPILATOR CB-2, Substantially Equivalent on 1983-01-14. Applicant: R. A. Fischer Co. Corp.. Device class: 1.

Clearance details

Applicant: R. A. Fischer Co. Corp.
Product code: Code KCW
Device class: Class 1
Regulation: 21 CFR 878.5350
Advisory panel: General, Plastic Surgery
Date received: 1982-12-07
Decision date: 1983-01-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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