VERIFY ASSERT STEAM Process Challenge Device for Gravity Cycles

VERIFY ASSERT STEAM Process Challenge Device for Gravity Cycles is an FDA 510(k)-cleared medical device (K170070) 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 April 27, 2017. Regulation: 8.