MODIFIED ASAHI PAN-SERIES HEMOFILTERS

MODIFIED ASAHI PAN-SERIES HEMOFILTERS is an FDA 510(k)-cleared medical device (K914020) manufactured by Asahi Medical Co., 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 March 19, 1992. Regulation: 8.