INTERSEPT* CRYSTALLOID CARDIOPLEGIA DELIV. SYSTEM

INTERSEPT* CRYSTALLOID CARDIOPLEGIA DELIV. SYSTEM is an FDA 510(k)-cleared medical device (K885154) manufactured by Medtronic Blood Systems, 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 February 21, 1989. Regulation: 8.