MODEL SE-5 EPILATOR— 510(k) K893389

Substantially Equivalent

R. A. Fischer Co. Corp.

FDA 510(k) clearance K893389 for MODEL SE-5 EPILATOR, Substantially Equivalent on 1989-06-05. Applicant: R. A. Fischer Co. Corp..

Clearance details

Applicant: R. A. Fischer Co. Corp.
Product code: Code KCW
Advisory panel: General, Plastic Surgery
Date received: 1989-05-01
Decision date: 1989-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Glendale, CA, US

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