PRESTIGE MEDICAL SERIES 2100 CLINICAL AUTOCLAVE

PRESTIGE MEDICAL SERIES 2100 CLINICAL AUTOCLAVE is an FDA 510(k)-cleared medical device (K962903) manufactured by Prestige Medical Corp.. 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 March 2, 1998. Regulation: 8.