EOPA ELONGATED ONE-PIECE ARTERIAL CANNULA AND GUIDEWIRE

EOPA ELONGATED ONE-PIECE ARTERIAL CANNULA AND GUIDEWIRE is an FDA 510(k)-cleared medical device (K031037) manufactured by Medtronic Perfusion Systems. 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 12, 2003. Regulation: 8.