K-number	K033982
Device name	MODIFICATION TO VYSIS UROVYSION BLADDER CANCER RECURRENCE TEST
Applicant	Vysis
Product code	MMW
Device class	Class II
Decision date	Jan 22, 2004
Decision	Substantially Equivalent
Regulation	866.6010

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MODIFICATION TO VYSIS UROVYSION BLADDER CANCER RECURRENCE TEST

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