CHASE RETROGRADE CARDIOPLEGIA CANNULA

CHASE RETROGRADE CARDIOPLEGIA CANNULA is an FDA 510(k)-cleared medical device (K964393) manufactured by Chase 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 April 22, 1997. Regulation: 8.