4F NYLEX ANGIOGRAPHIC CATHETER

4F NYLEX ANGIOGRAPHIC CATHETER is an FDA 510(k)-cleared medical device (K962759) 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 9, 1996. Regulation: 8.