DEPILATORY, ELECTRONIC— 510(k) K772322

Substantially Equivalent

Dura Corp., The

FDA 510(k) clearance K772322 for DEPILATORY, ELECTRONIC, Substantially Equivalent on 1978-01-03. Applicant: Dura Corp., The.

Clearance details

Applicant: Dura Corp., The
Product code: Code KCX
Advisory panel: General, Plastic Surgery
Date received: 1977-12-19
Decision date: 1978-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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