LILLIPUT 2 INFANT HOLLOW FIBER OXYGENATOR

LILLIPUT 2 INFANT HOLLOW FIBER OXYGENATOR is an FDA 510(k)-cleared medical device (K971877) 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 October 7, 1997. Regulation: 8.