ARS ENTERPRISES NEW/REMFR'D GP STEAM STERILIZER 81

ARS ENTERPRISES NEW/REMFR'D GP STEAM STERILIZER 81 is an FDA 510(k)-cleared medical device (K852113) manufactured by Ars Enterprises, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 26, 1985. Regulation: 8.