FDA 510(k) Applications Submitted by SARA L COON

FDA 510(k) Number	Submission Date	Device Name	Applicant
K050168	01/26/2005	LANGSTON DUAL LUMEN PRESSURE MONITORING CATHETER	VASCULAR SOLUTIONS, INC.
K060960	04/07/2006	BOSTON SCIENTIFIC TALON BALLOON DILATATION CATHETER	Boston Scientific Corporation
K051193	05/10/2005	VASCULAR SOLUTIONS PRONTO SHORT EXTRACTION CATHETER	VASCULAR SOLUTIONS, INC.
K051395	05/27/2005	LANGSTON DUAL LUMEN PRESSURE MONITORING CATHETER	VASCULAR SOLUTIONS, INC.
K041909	07/15/2004	VASCULAR SOLUTIONS LANGSTON DUAL LUMEN PIGTAIL CATHETER (DLP)	VASCULAR SOLUTIONS, INC.
K052232	08/17/2005	VASCULAR SOLUTIONS PRONTO V3 EXTRACTION CATHETER	VASCULAR SOLUTIONS, INC.
K052257	08/18/2005	VASCULAR SOLUTIONS TWIN-PASS DUAL ACCESS CATHETER	VASCULAR SOLUTIONS, INC.
K052258	08/19/2005	VASCULAR SOLUTIONS SKYWAY SUPPORT CATHETER	VASCULAR SOLUTIONS, INC.
K043019	11/03/2004	VASCULAR SOLUTIONS SCLERO-KIT	VASCULAR SOLUTIONS, INC.
K033721	11/26/2003	VASCULAR SOLUTIONS AUTO-FILL SYRINGE KIT	VASCULAR SOLUTIONS, INC.