NMI ANTEGRAD CARDIOPLEGIA CANNULA

NMI ANTEGRAD CARDIOPLEGIA CANNULA is an FDA 510(k)-cleared medical device (K961180) manufactured by Naltiac 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 June 20, 1996. Regulation: 8.