LEOCOR CORFLO PUMP -- MODIFICATION

LEOCOR CORFLO PUMP -- MODIFICATION is an FDA 510(k)-cleared medical device (K924110) 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 August 31, 1992. Regulation: 8.