EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIR

EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIR is an FDA 510(k)-cleared medical device (K823733) manufactured by Advocacy International, Ltd.. 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 January 13, 1983. Regulation: 8.