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Accumetrics, Inc.

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K051231	VERIFYNOW-P2Y12 ASSAY	JOZ	2005-08-05	View
510(k)	K042423	VERIFYNOW-ASPIRIN ASSAY	JOZ	2004-10-06	View
510(k)	K012701	ULTEGRA SYSTEM RAPID PLATELET FUNCTION ASSAY - ASA (RPFA-ASA)	JOZ	2002-06-12	View
510(k)	K013596	MODIFICATION TO ULTEGRA SYSTEM RAPID PLATELET FUNCTION ASSAY - TRAP (RPFA-TRAP)	JOZ	2002-05-16	View
510(k)	K011337	ULTEGRA SYSTEM RAPID PLATELET FUNCTION ASSAY (RPFA)	JOZ	2001-10-16	View
510(k)	K992531	ULTEGRA SYSTEM ANALYZER, ULTEGRA SYSTEM RPFA-TRAP TEST CARTIDGES, ULTEGRA SYSTEM RPFA-TRAP LEVEL ONE QC, ULTEGRA SYSTEM	JOZ	1999-12-20	View

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