EOPA 3D Arterial Cannula

EOPA 3D Arterial Cannula is an FDA 510(k)-cleared medical device (K150422) 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 March 19, 2015. Regulation: 8.