AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM

AMSCO V-PRO MAX LOW TEMPERATURE STERILIZATION SYSTEM is an FDA 510(k)-cleared medical device (K102330) manufactured by STERIS Corporation. 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 11, 2011. Regulation: 8.