PARAGON 8500 CARDIO-PULMONARY BED

PARAGON 8500 CARDIO-PULMONARY BED is an FDA 510(k)-cleared medical device (K872924) manufactured by Surgi-Med, Inc.. 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 October 8, 1987. Regulation: 8.