FDA 510(k) Applications Submitted by JODI L GREENIZEN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K020012	01/03/2002	MODIFICATION TO RENEGADE FIBER BRAIDED MICROCATHETER	BOSTON SCIENTIFIC/MEDI-TECH
K011664	05/30/2001	IMAGER II ANGIOGRAPHIC CATHETER	BOSTON SCIENTIFIC/MEDI-TECH
K003929	12/20/2000	NIROYAL BILIARY PREMOUNTED STENT SYSTEM	BOSTON SCIENTIFIC CORP.
K030083	01/09/2003	VAXCEL WITH PASV PORT	BOSTON SCIENTIFIC CORP.
K971010	03/20/1997	PERIPHERAL TRANSLUMINAL ANGIOPLASTY CATHETERS	CORDIS CORP.
K030966	03/27/2003	CONTOUR EMBOLI PVA AND FASTRACKER-325 INFUSION CATHETER	BOSTON SCIENTIFIC CORP.
K971579	04/21/1997	CORDIS OPTA 5 PTA BALLOON CATHETER	CORDIS CORP.
K031844	06/16/2003	VAXCEL WITH PASV PORT (LOW PROFILE), MODELS 45-236 AND 45-238	BOSTON SCIENTIFIC CORP.
K011906	06/19/2001	BACK-UP MEIER GUIDEWIRE	BOSTON SCIENTIFIC CORP.
K032008	06/30/2003	VAXCEL WITH PASV PORT, MODEL 45-213	BOSTON SCIENTIFIC CORP.
K022427	07/25/2002	CONTOUR SE MICROSPHERES	BOSTON SCIENTIFIC CORP.
K032375	08/01/2003	VAXCEL PORT, MODELS 45-336 AND 45-338	BOSTON SCIENTIFIC CORP.
K032542	08/18/2003	MODIFICATION TO CONTOUR SE MICROSPHERES	BOSTON SCIENTIFIC CORP.
K032600	08/25/2003	VAXCEL PORT, MODEL 45-333 AND VAXCEL W/PASV PORT, MODEL 45-233	BOSTON SCIENTIFIC CORP.
K032707	09/02/2003	CONTOUR SE MICROSPHERES (SYRINGE)	BOSTON SCIENTIFIC CORP.