LEOCOR CORFLO(TM) PUMP

LEOCOR CORFLO(TM) PUMP is an FDA 510(k)-cleared medical device (K900350) manufactured by Leocor, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 16, 1990. Regulation: 8.