
STERIS Corporation
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enspire 3000 Cleaning and Liquid Chemical Sterile Processing System is an FDA 510(k)-cleared medical device (K230930) manufactured by STERIS Corporation. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 29, 2023. Regulation: 8.