American Diagnostica, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Diagnostica, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
American Diagnostica, Inc. has 10 FDA 510(k) cleared hematology devices. Based in Greenwich, US.
Historical record: 10 cleared submissions from 1994 to 2008.
Browse the complete list of FDA 510(k) cleared hematology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Diagnostica, Inc.
10 devices
Cleared
Feb 13, 2008
DIMERTEST
Hematology
34d
Cleared
Aug 15, 2007
SPECTROLYSE PAI-1, MODEL 101201
Hematology
285d
Cleared
Oct 17, 2005
ACTICLOT, MODEL 824
Hematology
73d
Cleared
Apr 16, 2002
ACTICHROME HEPARIN (ANTI-FIIA)
Hematology
162d
Cleared
Mar 13, 2002
IMUBIND TPA ELISA, MODEL 860
Hematology
142d
Cleared
Mar 08, 2002
ACTICHROME HEPARIN (ANTI-FXA), MODEL 832
Hematology
154d
Cleared
Mar 07, 2002
IMUBIND PLASMA PAI-1 ELISA,MODEL 822
Hematology
167d
Cleared
Sep 14, 2001
ACTICLOT PROTEIN S, MODEL 843L
Hematology
49d
Cleared
Apr 05, 1995
DV TEST AND DVV CONFIRM
Hematology
426d
Cleared
Sep 19, 1994
DVVTEST AND DVVCONFIRM LUPUS ANTICOAGULANT NORMAL AND ABNORMAL CONTROL PLASMA
Hematology
322d