FDA 510(k) Applications Submitted by HAEMOSCOPE CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K954437 09/22/1995 THROMBELASTOGRAPH COAGULATION ANALYZER 3000S HAEMOSCOPE CORP.
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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