HEARTPORT ENDOVENOUS DRAINAGE CANNULA

HEARTPORT ENDOVENOUS DRAINAGE CANNULA is an FDA 510(k)-cleared medical device (K962835) manufactured by Heartport, 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 February 9, 1997. Regulation: 8.