Thoratec CentriMag Return (Arterial) Cannula Kit

Thoratec CentriMag Return (Arterial) Cannula Kit is an FDA 510(k)-cleared medical device (K152161) manufactured by Thoratec Corporation. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 17, 2015. Regulation: 8.