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Vysis

FDA 510(k) & PMA Approved Devices — 8 products

Total Devices8

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K033982	MODIFICATION TO VYSIS UROVYSION BLADDER CANCER RECURRENCE TEST	MMW	2004-01-22	View
510(k)	K013785	UROVYSION BLADDER CANCER RECURRENCE KIT	MMW	2002-02-08	View
510(k)	K011031	VYSIS UROVYSION BLADDER CANCER RECURRENCE KIT	MMW	2001-08-03	View
510(k)	K010288	ANEUVYSION MULITICOLOR DNA PROBE KIT	OYU	2001-04-13	View
510(k)	K972200	ANEUVYSION	OYU	1997-10-20	View
510(k)	K954214	CEP X SPECTRUMORANGE\Y SPECTRUMGREEN DNA PROBE KIT	OXP	1997-01-21	View
510(k)	K962873	CEP 12 SPECTRUMORANGE DIRECT LABELED CHROMOSOME ENUMERATION DNA PROBE	OVQ	1997-01-13	View
510(k)	K953591	CEP 8 SPECTRUMORANGE DNA PROBE KIT	OYU	1996-11-29	View

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