DUODERM HYDROCOLLOID GEL

DUODERM HYDROCOLLOID GEL is an FDA 510(k)-cleared medical device (K931618) manufactured by Convatec, A Division of E.R. Squibb & Sons. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 9, 1993. Regulation: 8.