Multi-Sideport Catheter Infusion Set

Multi-Sideport Catheter Infusion Set is an FDA 510(k)-cleared medical device (K182071) manufactured by Cook Incorporated. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 24, 2019. Regulation: 8.