DIDECO D920, LILLIPUT 1 TWIN RESERVOIR

DIDECO D920, LILLIPUT 1 TWIN RESERVOIR is an FDA 510(k)-cleared medical device (K984322) 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 March 1, 1999. Regulation: 8.