FOAMSEAL RETROGRADE CARDIOPLEGIA CATHETER

FOAMSEAL RETROGRADE CARDIOPLEGIA CATHETER is an FDA 510(k)-cleared medical device (K955818) 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 March 25, 1996. Regulation: 8.