FDA 510(k) Applications Submitted by GUIDANT CORPORATION

FDA 510(k) Number	Submission Date	Device Name	Applicant
K041574	06/14/2004	CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020	GUIDANT CORPORATION
K041762	06/30/2004	FINISHING WIRE SUPPORTRAK	GUIDANT CORPORATION
K060449	02/21/2006	HI-TORQUE ADVANCE AND ADVANCE LITE GUIDE WIRE	GUIDANT CORPORATION
K053019	10/26/2005	ACUITY STEERABLE STYLET ACCESSORY	GUIDANT CORPORATION
K052165	08/09/2005	RX ACCUNET EMBOLIC PROTECTION SYSTEM	GUIDANT CORPORATION
K052166	08/09/2005	MODIFICATION TO: RX ACCUNET EMBOLIC PROTECTION SYSTEM	GUIDANT CORPORATION
K053454	12/09/2005	RX HERCULINK ELITE BILIARY STENT SYSTEM	GUIDANT CORPORATION
K052965	10/21/2005	EASYTRAK 2 STYLET, MODELS 4826, 4829, 4832.	GUIDANT CORPORATION
K041981	07/23/2004	GUIDANT VASOVIEW 6 HARVESTING CANNULA, MODEL VH-2000; GUIDANT VASOVIEW 6 ACCESSORY PACK, MODEL VH-2004	GUIDANT CORPORATION
K052274	08/22/2005	GUIDANT VASOVIEW HEMOPRO ENDOSCOPIC VESSEL HARVESTING SYSTEM, MODEL VH-3000	GUIDANT CORPORATION
K032530	08/15/2003	MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM	GUIDANT CORPORATION
K031505	05/14/2003	RAPIDO CUT-AWAY GUIDING CATHETER	GUIDANT CORPORATION
K031688	06/02/2003	RAPIDO CUT-A-WAY ROTATING HEMOSTASIS VALVE	GUIDANT CORPORATION
K031903	06/20/2003	RAPIDO CUT-AWAY BLEEDBACK CONTROL VALVE (BBCV), MODEL 7568	GUIDANT CORPORATION
K053459	12/13/2005	OMNILINK .035 BILIARY STENT SYSTEM	GUIDANT CORPORATION