FDA 510(k) Applications for Medical Device Product Code: GFX (Fibrinogen Standard)

FDA 510(k) Applications for Medical Device Product Code "GFX"
(Fibrinogen Standard)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K994341	DADE BEHRING, INC.	FIBRINOGEN CALIBRATOR KIT	03/03/2000
K072304	DADE BEHRING, INC.	FIBRINOGEN CALIBRATOR KIT	09/19/2007

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