Chrono-Log Corp. is one of 4740 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Chrono-Log Corp. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Chrono-Log Corp. has 16 FDA 510(k) cleared hematology devices. Based in Havertown, US.
Historical record: 16 cleared submissions from 1976 to 2016.
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 - Chrono-Log Corp.
16 devices
Cleared
Dec 02, 2016
Chrono-log Platelet Aggregometer, 4 channel
Hematology
204d
Cleared
Oct 14, 2005
CHRONO-LOG WHOLE BLOOD LUMI-AGGREGOMETER, MODEL 700
Hematology
252d
Cleared
Apr 02, 2004
CHRONO-LOG WHOLE BLOOD AGGREGOMETER, MODELS 591A AND 592A
Hematology
193d
Cleared
Oct 22, 1996
CHRONO-LOG WHOLE BLOOD AGGREGOMETER (WBA) 591/592
Hematology
120d
Cleared
Jan 11, 1995
RISTOCETIN COFACTOR ASSAY KIT
Hematology
65d
Cleared
Oct 13, 1994
AGGRO/LINK VW COFACTOR SOFTWARE
Hematology
233d
Cleared
Nov 02, 1993
AGGRO/LINK CONTROL SOFTWARE
Hematology
159d
Cleared
Aug 26, 1992
PLATELET AGGREGATION REAGENTS
Hematology
77d
Cleared
Jun 12, 1985
AGGRO/LINK COMPUTER INTERFACE
Hematology
93d
Cleared
May 13, 1985
PLATELET AGGREGATION REAGENT
Hematology
87d
Cleared
May 16, 1983
PLATELET AGGREGOMETER
Hematology
68d
Cleared
Mar 16, 1982
PLATELET AGGREGOMETERS
Hematology
28d
Cleared
Nov 22, 1978
REAGENT, FIREFLY #395
Hematology
28d
Cleared
Aug 02, 1977
LUMI-AGGREGOMETER
Hematology
32d
Cleared
Jul 20, 1976
AGGREGOMETER, DUAL CHANNEL PLATELET
Hematology
18d
Cleared
Jul 19, 1976
KIT, PLATELET AGGREGATION REAGENT (#390)
Hematology
13d