PERIPHERAL RETROGRADE CARDIAPLEGIA CANNULA

PERIPHERAL RETROGRADE CARDIAPLEGIA CANNULA is an FDA 510(k)-cleared medical device (K983791) manufactured by Edwards Lifesciences Research Medical. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 10, 1999. Regulation: 8.