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Chrono-Log Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
16
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K161329Chrono-log Platelet Aggregometer, 4 channel; Chrono-log Platelet Aggregometer, 8 channelDecember 2, 2016
K050265CHRONO-LOG WHOLE BLOOD LUMI-AGGREGOMETER, MODEL 700October 14, 2005
K032951CHRONO-LOG WHOLE BLOOD AGGREGOMETER, MODELS 591A AND 592AApril 2, 2004
K962426CHRONO-LOG WHOLE BLOOD AGGREGOMETER (WBA) 591/592October 22, 1996
K945414RISTOCETIN COFACTOR ASSAY KITJanuary 11, 1995
K940792AGGRO/LINK VW COFACTOR SOFTWAREOctober 13, 1994
K932566AGGRO/LINK CONTROL SOFTWARENovember 2, 1993
K922800PLATELET AGGREGATION REAGENTSAugust 26, 1992
K851025AGGRO/LINK COMPUTER INTERFACEJune 12, 1985
K850592PLATELET AGGREGATION REAGENTMay 13, 1985
K830749PLATELET AGGREGOMETERMay 16, 1983
K820422PLATELET AGGREGOMETERSMarch 16, 1982
K781807REAGENT, FIREFLY #395November 22, 1978
K771198LUMI-AGGREGOMETERAugust 2, 1977
K760159AGGREGOMETER, DUAL CHANNEL PLATELETJuly 20, 1976
K760198KIT, PLATELET AGGREGATION REAGENT (#390)July 19, 1976