FDA Product Code DAP: Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control
Under FDA product code DAP, fibrinogen and fibrin split product antigen/antibody detection systems are cleared for the evaluation of coagulation disorders.
These tests measure fibrin degradation products and D-dimer in plasma to detect excessive fibrinolysis, disseminated intravascular coagulation, and venous thromboembolism. Elevated FDP and D-dimer indicate ongoing coagulation and fibrinolysis activity.
DAP devices are Class II medical devices, regulated under 21 CFR 864.7320 and reviewed by the FDA Hematology panel.
Leading manufacturers include Instrumentation Laboratory CO, Dade Behring, Inc. and Organon Teknika Corp..
58
Total
58
Cleared
139d
Avg days
1986
Since
58 devices
Cleared
Nov 02, 1993
FIBRIN(OGEN) FDP CONTROL LEVEL 1 & LEVEL 2
More Diagnostics
Hematology
153d
Cleared
Aug 05, 1992
FIBRINOSTIKA TDP MICROELISA SYSTEM
Organon Teknika Corp.
Hematology
226d
Cleared
Jul 13, 1992
FDP PLASMA TEST KIT
American Bioproducts Co.
Hematology
137d
Cleared
Jan 31, 1992
D-DIMER WELLCOTEST (HA10)
Wellcome Diagnostics
Hematology
74d
Cleared
Jan 30, 1992
FIBRINOGEN FDP CONTROL
Cala Diagnostics
Hematology
52d
Cleared
Oct 09, 1991
FIBRINOSTIKA FBDP MICROELISA SYSTEM
Organon Teknika Corp.
Hematology
100d
Cleared
Mar 03, 1989
AGEN DIMERTEST EIA
Agen Biomedical , Ltd.
Hematology
45d
Cleared
Aug 17, 1988
DIMERTEST(R) LATEX
Agen Biomedical , Ltd.
Hematology
34d
Cleared
Aug 06, 1987
DATA-FI DIMERTEST LATEX ASSAY
American Dade
Hematology
59d
Cleared
Sep 16, 1986
ASSERACHROM D-DI KIT
American Bioproducts Co.
Hematology
103d