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FDA 510(k) Applications Submitted by ELI COHEN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K041502
06/07/2004
THROMBELASTOGRAPH (TEG) PLATELET MAPPING ASSAY
HAEMOSCOPE CORP.
K002177
07/19/2000
THROMBELASTOGRAPH COAGULATION ANALYZER TEG-5000 SERIES
HAEMOSCOPE CORP.
K062604
09/01/2006
RAPIDTEG TEG-ACT TEST
HAEMOSCOPE CORP.
K993678
11/01/1999
THROMBELASTOGRAPH COAGULATION ANALYZER TEG - 5000 SERIES
HAEMOSCOPE CORP.
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