CORDIS 8 FRENCH 0.084 I.D. PTCA GUIDING CATHETER

CORDIS 8 FRENCH 0.084 I.D. PTCA GUIDING CATHETER is an FDA 510(k)-cleared medical device (K911703) 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 June 27, 1991. Regulation: 8.