MODIFIED SEPACELL R-SERIES BLOOD FILTERS

MODIFIED SEPACELL R-SERIES BLOOD FILTERS is an FDA 510(k)-cleared medical device (K901887) manufactured by Asahi Medical Co., Ltd.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 7, 1990. Regulation: 8.