QBC FIBRINOGEN

QBC FIBRINOGEN is an FDA 510(k)-cleared medical device (K920258) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 25, 1992. Regulation: 8.