CARPENTIER BI-CAVAL FEMORAL CANNULA

CARPENTIER BI-CAVAL FEMORAL CANNULA is an FDA 510(k)-cleared medical device (K140192) manufactured by Medtronic, 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 21, 2014. Regulation: 8.