
Medtronic Cardiac Surgical Products
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MEDTRONIC DLP ARTERIAL CANNULA WITH 3D TIP - 22 FR. is an FDA 510(k)-cleared medical device (K013013) manufactured by Medtronic Cardiac Surgical Products. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 3, 2001. Regulation: 8.