CELERITY 20 Steam Process Challenge Device for Gravity Cycles

CELERITY 20 Steam Process Challenge Device for Gravity Cycles is an FDA 510(k)-cleared medical device (K173629) 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 February 20, 2018. Regulation: 8.