CORDIS DOW C-DAK 1.3MRC ARTIF. KIDNEY

CORDIS DOW C-DAK 1.3MRC ARTIF. KIDNEY is an FDA 510(k)-cleared medical device (K802893) manufactured by Cordis Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 12, 1981. Regulation: 8.