
Medtronic Perfusion Systems
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SELECT 3D ARTERIAL CANNULA is an FDA 510(k)-cleared medical device (K043179) 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 February 7, 2005. Regulation: 8.