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FDA 510(k) Applications Submitted by NICHOLAS J VERIABO
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050265
02/04/2005
CHRONO-LOG WHOLE BLOOD LUMI-AGGREGOMETER, MODEL 700
CHRONO-LOG CORP.
K161329
05/12/2016
Chrono-log Platelet Aggregometer, 4 channel; Chrono-log Platelet Aggregometer, 8 channel
Chrono-log Corp.
K962426
06/24/1996
CHRONO-LOG WHOLE BLOOD AGGREGOMETER (WBA) 591/592
CHRONO-LOG CORP.
K032951
09/22/2003
CHRONO-LOG WHOLE BLOOD AGGREGOMETER, MODELS 591A AND 592A
CHRONO-LOG CORP.
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