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Horizon Diagnostics, Inc.

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K971566	CREATINE KINASE-MB REAGENT SET	CGS	1997-07-14	View
510(k)	K933722	HORIZON DIAGNOSTICS TRIGLYCERIDES-GPO REAGENT	CDT	1996-06-13	View
510(k)	K935712	IRON/TIBC REAGENT	JIY	1995-09-20	View
510(k)	K930678	AMYLASE	JFJ	1994-04-06	View
510(k)	K934533	BUN-300/BUN-500 UREA NITROGEN REAGENT	CDQ	1993-11-26	View
510(k)	K930679	DIRECT BILIRUBIN	CIG	1993-06-29	View
510(k)	K930074	IN-VITRO DIAGNOSTIC REAGENT SET	JGJ	1993-05-11	View

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