DEPILATOR, DERMA-I & DERMA-II

DEPILATOR, DERMA-I & DERMA-II is an FDA 510(k)-cleared medical device (K770791) manufactured by Electro-Kinetic Eng/Mfg. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 25, 1981. Regulation: 8.