FDA 510(k) Applications Submitted by HEMOSENSE, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K072727 09/26/2007 INRATIO 2 PT MONITORING SYSTEM HEMOSENSE, INC.
K020679 03/04/2002 INRATIO HEMOSENSE, INC.
K021923 06/11/2002 INRATIO SELF-TEST HEMOSENSE, INC.


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