PARADERM(TM) SURGEON'S GLOVE ACCESSORY

PARADERM(TM) SURGEON'S GLOVE ACCESSORY is an FDA 510(k)-cleared medical device (K904903) manufactured by Lovell-Schenck, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 7, 1991. Regulation: 8.