CORDIS 6 FRENCH 0.062 I.D. PTCA GUIDING CATHTER

CORDIS 6 FRENCH 0.062 I.D. PTCA GUIDING CATHTER is an FDA 510(k)-cleared medical device (K915374) 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 February 13, 1992. Regulation: 8.