EPILATOR— 510(k) K952117

Substantially Equivalent

Burke Neutech, Inc.

FDA 510(k) clearance K952117 for EPILATOR, Substantially Equivalent on 1995-10-19. Applicant: Burke Neutech, Inc..

Clearance details

Applicant: Burke Neutech, Inc.
Product code: Code KCX
Advisory panel: General, Plastic Surgery
Date received: 1995-05-05
Decision date: 1995-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Petersburg, FL, US

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