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Dako Diagnostics , Ltd.

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

Total Devices6

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K981226	IMAGEARAINFLUENZA VIRUS GROUP (TYPES 1,2 AND 3) TEST AND IMAGEN PARAINFLUENZA VIRUS TEST TYPES 1,2 AND 3	GQP	1998-09-28	View
510(k)	K973954	IMAGEN RESPIRATORY SCREEN	GNW	1997-12-22	View
510(k)	K962037	IMAGEN RESPIRATORY SCREEN	GNW	1996-12-26	View
510(k)	K940564	IDEIA(TM) CHLAMYDIA BLOCKING REAGENTS, MODIFICATION	LJC	1996-01-11	View
510(k)	K943557	IMAGEN	GQS	1995-01-09	View
510(k)	K932384	IDEIA(TM) ROTAVIRUS	LIQ	1993-12-27	View

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