SPYROSORB FOAM ISLAND WOUND DRESSING

SPYROSORB FOAM ISLAND WOUND DRESSING is an FDA 510(k)-cleared medical device (K980673) manufactured by Innovative Technologies (Us), Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 20, 1998. Regulation: 8.