RESUBMITTED STC SERIES 8600 AUTOCLAVE

RESUBMITTED STC SERIES 8600 AUTOCLAVE is an FDA 510(k)-cleared medical device (K890359) manufactured by Sterilizer Technologies Corp.. 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 August 6, 1989. Regulation: 8.