Protek Solo 24 Fr Venous Cannula Set

Protek Solo 24 Fr Venous Cannula Set is an FDA 510(k)-cleared medical device (K162214) manufactured by Cardiacassist, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 29, 2016. Regulation: 8.