PYNE/CHEMO-TOUCH, ULTRA-SHIELD, PYNE-STERIE, MODIF

PYNE/CHEMO-TOUCH, ULTRA-SHIELD, PYNE-STERIE, MODIF is an FDA 510(k)-cleared medical device (K914628) manufactured by Medical Resources, Ltd.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 6, 1991. Regulation: 8.