CORDIS DUAL LUMEN PRESSURE MONITORING CATHETER

CORDIS DUAL LUMEN PRESSURE MONITORING CATHETER is an FDA 510(k)-cleared medical device (K914141) manufactured by Cordis Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 22, 1991. Regulation: 8.