LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR

LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR is an FDA 510(k)-cleared medical device (K953835) manufactured by Dideco S.R.L.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 14, 1996. Regulation: 8.