D903 AVANT ADULT HOLLOW FIBER OXYGENATOR

D903 AVANT ADULT HOLLOW FIBER OXYGENATOR is an FDA 510(k)-cleared medical device (K980600) manufactured by Dideco S.P.A.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 11, 1998. Regulation: 8.