CODMAN STERILIZATION CONTAINERS

CODMAN STERILIZATION CONTAINERS is an FDA 510(k)-cleared medical device (K092437) manufactured by Codman & Shurtleff, 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 March 24, 2010. Regulation: 8.