HEARTPORT ENDOAORTIC CLAMP CATHETER

HEARTPORT ENDOAORTIC CLAMP CATHETER is an FDA 510(k)-cleared medical device (K974175) 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 December 15, 1997. Regulation: 8.