HEMOSIL LIQUID ANTITHROMBIN XL

HEMOSIL LIQUID ANTITHROMBIN XL is an FDA 510(k)-cleared medical device (K033775) manufactured by Instrumentation Laboratory CO. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 1, 2004. Regulation: 8.