STERILIZER, SERIES 3000, MODIFICATION TO

STERILIZER, SERIES 3000, MODIFICATION TO is an FDA 510(k)-cleared medical device (K770682) manufactured by Castle Co.. 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 May 19, 1977. Regulation: 8.