SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model 6900

SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model 6900 is an FDA 510(k)-cleared medical device (K182827) 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 January 30, 2019. Regulation: 8.