FDA 510(k) Applications Submitted by SUSAN SCOTT

FDA 510(k) Number	Submission Date	Device Name	Applicant
K090084	01/12/2009	ELATION ENDOVENOUS LASER PROCEDURE KIT UNIVERSAL FLUID DISPENSING SYRINGE	MERIT MEDICAL SYSTEMS, INC.
K060812	03/24/2006	POWERPORT(TM)IMPLANTED TITANIUM PORT W/8 FR. CHRONOFLEX CATHETER-MULTIPLE	C.R. BARD, INC.
K063118	10/11/2006	BARD BALLOON DILATION KIT WITH TRIFUNNEL GASTROSTOMY TUBE	C.R. BARD, INC.
K072215	08/09/2007	TITANIUM POWERPORT ISP IMPLANTED PORT	C.R. BARD, INC.
K072549	09/10/2007	TITANIUM POWERPORT ISP IMPLANTED PORT WITH 6 FR CHRONOFLEX POLYURETHANE CATHETER	C.R. BARD, INC.
K083523	11/26/2008	MONARCH COMPAK INFLATION SYRINGE AND UNIVERSAL FLUID DISPENSING SYRINGE	MERIT MEDICAL SYSTEMS, INC.
K073423	12/05/2007	MRI POWERPORT IMPLANTED PORT WITH 9.6 FR SILICONE CATHETER	C.R. BARD, INC.