ACTIDERM (TM) DERMATOLOGICAL PATCH

ACTIDERM (TM) DERMATOLOGICAL PATCH is an FDA 510(k)-cleared medical device (K895376) manufactured by Convatec, A Division of E.R. Squibb & Sons. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 24, 1989. Regulation: 8.