HEARTPORT ENDOARTERIAL RETURN CANNUAL

HEARTPORT ENDOARTERIAL RETURN CANNUAL is an FDA 510(k)-cleared medical device (K955121) 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 May 9, 1996. Regulation: 8.