EOPA 3D ARTERIAL CANNULA, MODELS 78220,78222,78320,783222

EOPA 3D ARTERIAL CANNULA, MODELS 78220,78222,78320,783222 is an FDA 510(k)-cleared medical device (K061254) 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 June 22, 2006. Regulation: 8.