FDA 510(k) Applications Submitted by RHONDA MOE

FDA 510(k) Number Submission Date Device Name Applicant
K011337 05/02/2001 ULTEGRA SYSTEM RAPID PLATELET FUNCTION ASSAY (RPFA) ACCUMETRICS, INC.
K012701 08/14/2001 ULTEGRA SYSTEM RAPID PLATELET FUNCTION ASSAY - ASA (RPFA-ASA) ACCUMETRICS, INC.
K013596 10/31/2001 MODIFICATION TO ULTEGRA SYSTEM RAPID PLATELET FUNCTION ASSAY - TRAP (RPFA-TRAP) ACCUMETRICS, INC.


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