CORDIS 6 FRENCH PARAGON ANGIOGRAPHIC CATHETER

CORDIS 6 FRENCH PARAGON ANGIOGRAPHIC CATHETER is an FDA 510(k)-cleared medical device (K921310) 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 September 16, 1992. Regulation: 8.