VERIFY SPORE TEST STRIP for S40 STERILANT CONCENTRATE

VERIFY SPORE TEST STRIP for S40 STERILANT CONCENTRATE is an FDA 510(k)-cleared medical device (K233682) 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 December 14, 2023. Regulation: 8.