MC3 Jugular Dual Lumen Catheter

MC3 Jugular Dual Lumen Catheter is an FDA 510(k)-cleared medical device (K180151) manufactured by Mc3 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 July 15, 2018. Regulation: 8.