CORDIS 9 F GUIDING CATHETER

CORDIS 9 F GUIDING CATHETER is an FDA 510(k)-cleared medical device (K925131) 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 May 5, 1993. Regulation: 8.