CLEARSITE HYDROGEL WOUND DRESSING MODIFICATION

CLEARSITE HYDROGEL WOUND DRESSING MODIFICATION is an FDA 510(k)-cleared medical device (K920677) manufactured by New Dimensions IN Medicine, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 20, 1992. Regulation: 8.