QUEST ANTEGRADE CARDIOPLEGIA CANNULA

QUEST ANTEGRADE CARDIOPLEGIA CANNULA is an FDA 510(k)-cleared medical device (K950814) manufactured by Quest Medical, 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 May 24, 1995. Regulation: 8.