CORDIS ANGIOPLASTY HEMOSTASIS DEVICES

CORDIS ANGIOPLASTY HEMOSTASIS DEVICES is an FDA 510(k)-cleared medical device (K863177) 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 14, 1986. Regulation: 8.