INTRASITE HYDROCOLLOID DRESSING (REVISED LABELING)

INTRASITE HYDROCOLLOID DRESSING (REVISED LABELING) is an FDA 510(k)-cleared medical device (K901879) manufactured by Smith & Nephew United, Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 21, 1990. Regulation: 8.