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Orion Diagnostica, Div. Orion Corp.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K031607	ORION DIAGNOSTICA QUIKREAD CRP KIT AND QUIKREAD CRP CONTROL	DCK	2003-10-10	View
510(k)	K022176	ORION DIAGNOSTICA ULTRASENSITIVE CRP KIT, MODEL 68025, & ORION DIAGNOSTICA ULTRASENSITIVE CRP CONTROL, MODEL 68257	DCK	2002-12-03	View
510(k)	K971537	PYLORISET EIA-G (68926)	LYR	1997-06-27	View
510(k)	K942974	PYLORISET DRY	LYR	1995-04-05	View

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