CENTRIMAG RETURN CANNULA KIT

CENTRIMAG RETURN CANNULA KIT is an FDA 510(k)-cleared medical device (K110980) manufactured by Levitronix, LLC. 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 19, 2011. Regulation: 8.