FDA 510(k) Applications Submitted by GARY M RAUVOLA

FDA 510(k) Number	Submission Date	Device Name	Applicant
K021363	04/30/2002	ENDOVASCULAR GUIDE WIRE	STEREOTAXIS, INC.
K042850	10/15/2004	CARDIODRIVE, MODEL 001-004115 (NON-STERILE); 001-1169-1 (STERILE)	STEREOTAXIS, INC.
K042854	10/15/2004	STEREOTAXIS ENDOVASCULAR GUIDE WIRE	STEREOTAXIS, INC.
K173480	11/13/2017	Crystalsert Lens Delivery System	Bausch & Lomb, Inc
K043457	12/15/2004	MODIFICATION TO ENDOVASCULAR GUIDE WIRE	STEREOTAXIS, INC.
K980488	02/09/1998	STORZ MILLENNIUM MICROSURGICL SYSTEM HIGH SPEED VITRECTOMY SYSTEM	STORZ INSTRUMENT CO.
K021802	06/03/2002	STEREOTAXIS CATHETER ADVANCER SYSTEM	STEREOTAXIS, INC.