CORDIS DOW C-DAK 1.8MRC ARTIFIC-KIDNEY

CORDIS DOW C-DAK 1.8MRC ARTIFIC-KIDNEY is an FDA 510(k)-cleared medical device (K802894) 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 18, 1981. Regulation: 8.