CURADERM ALGINATE HYDROCOLLOID

CURADERM ALGINATE HYDROCOLLOID is an FDA 510(k)-cleared medical device (K943636) manufactured by Kendall Healthcare Products Co. Div.Of Tyco Health. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 2, 1994. Regulation: 8.