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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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