CORDIS ANGIOGRAPHIC DOPPLER CATHER

CORDIS ANGIOGRAPHIC DOPPLER CATHER is an FDA 510(k)-cleared medical device (K915498) 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 April 16, 1992. Regulation: 8.