ALTERNATE STERILIZ. FOR CELLULOSE ACET

ALTERNATE STERILIZ. FOR CELLULOSE ACET is an FDA 510(k)-cleared medical device (K810315) manufactured by Cordis Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 19, 1981. Regulation: 8.