MODIFICATION OF KENDALL CURASORB CALCIUM ALGINATE WOUND DRESSING

MODIFICATION OF KENDALL CURASORB CALCIUM ALGINATE WOUND DRESSING is an FDA 510(k)-cleared medical device (K933689) 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 December 12, 1993. Regulation: 8.