DEPILATOR, DERMA-I & DERMA-II— 510(k) K770791

Substantially Equivalent

Electro-Kinetic Eng/Mfg

FDA 510(k) clearance K770791 for DEPILATOR, DERMA-I & DERMA-II, Substantially Equivalent on 1981-01-26. Applicant: Electro-Kinetic Eng/Mfg.

Clearance details

Applicant: Electro-Kinetic Eng/Mfg
Product code: Code KCX
Advisory panel: General, Plastic Surgery
Date received: 1977-05-02
Decision date: 1981-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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