
Clinical Controls, Inc.
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LIQUID FIBRINOGEN FDP CONTROL LEVEL 1 & 2 is an FDA 510(k)-cleared medical device (K934741) manufactured by Clinical Controls, Inc.. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 7, 1994. Regulation: 8.