Vysis

FDA Filings

This page includes the latest FDA filings for Vysis. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Filings

Device Company	Device	Date
De Novo DEN040010 VYSIS	VYSIS AUTOVYSION SYSTEM	2004-12-13
PMN K033982 VYSIS	MODIFICATION TO VYSIS UROVYSION BLADDER CANCER RECURRENCE TEST	2004-01-22
PMN K013785 VYSIS	UROVYSION BLADDER CANCER RECURRENCE KIT	2002-02-08
PMN K011031 VYSIS	VYSIS UROVYSION BLADDER CANCER RECURRENCE KIT	2001-08-03
PMN K010288 VYSIS	ANEUVYSION MULITICOLOR DNA PROBE KIT	2001-04-13
PMN K972200 VYSIS	ANEUVYSION	1997-10-20
PMN K954214 VYSIS	CEP X SPECTRUMORANGE\Y SPECTRUMGREEN DNA PROBE KIT	1997-01-21
PMN K962873 VYSIS	CEP 12 SPECTRUMORANGE DIRECT LABELED CHROMOSOME ENUMERATION DNA PROBE	1997-01-13
PMN K953591 VYSIS	CEP 8 SPECTRUMORANGE DNA PROBE KIT	1996-11-29