American Bioproducts Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Bioproducts Co. - FDA 510(k) Cleared Devices
79
Total
75
Cleared
0
Denied
American Bioproducts Co. has 75 FDA 510(k) cleared hematology devices. Based in Parsippany, US.
Historical record: 75 cleared submissions from 1985 to 1998.
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 Bioproducts Co.
79 devices
Cleared
Nov 12, 1998
STAR AUTOMATED MULTI-PARAMETRIC ANALYZER
Hematology
43d
Cleared
Aug 19, 1997
ASSERACHROM TPA TEST KIT
Hematology
116d
Cleared
Jun 26, 1997
STA LIATEST CONTROL [N]+[P] KIT
Hematology
213d
Cleared
Jun 26, 1997
STA-LIATEST D-DI TEST KIT
Hematology
213d
Cleared
May 23, 1997
STA D-DI CALIBRATOR KIT
Hematology
179d
Cleared
Oct 25, 1996
STA - LIATEST VWF TEST KIT
Hematology
108d
Cleared
Sep 13, 1996
STA-VWF CALIBRATOR KIT
Hematology
66d
Cleared
Jul 23, 1996
STA - VWF CONTROL [N]+[P] KIT
Hematology
14d
Cleared
Jul 10, 1996
STA COMPACT AUTOMATED MULTI-PARAMETRIC ANALYZER
Hematology
77d
Cleared
Jan 31, 1996
AT-III CONTROL PLASMA KIT
Hematology
89d
Cleared
Nov 13, 1995
ASSERACHROM FREE PROTEIN S KIT
Hematology
80d
Cleared
Nov 13, 1995
ASSERACHROM TOTAL PROTEIN S KIT
Hematology
77d
Looking for a specific device from American Bioproducts Co.? Search by device name or K-number.
Search all American Bioproducts Co. devices