FDA 510(k) Applications Submitted by Michael Ivey

FDA 510(k) Number	Submission Date	Device Name	Applicant
K130215	01/29/2013	GORE ACUSEAL VASCULAR GRAFT	W.L. GORE & ASSOCIATES,INC
K180919	04/09/2018	GORE Tri-Lumen Catheter	W.L. Gore and Associates Inc.
K081184	04/25/2008	GORE VIABIL BILILARY ENDOPROSTHESIS	W.L. GORE & ASSOCIATES INC, MEDICAL PRODUCTS DIV.
K041423	05/28/2004	VIABIL BILIARY ENDOPROSTHESIS	W. L. GORE & ASSOCIATES, INC.
K061727	06/19/2006	GORE PRECLUDE VESSEL GUARD	W.L. GORE & ASSOCIATES,INC
K062161	07/28/2006	GORE PROPATEN VASCULAR GRAFT	W.L. GORE & ASSOCIATES,INC
K043081	11/08/2004	GORE POLYPROPYLENE HERNIA MESH	W. L. GORE & ASSOCIATES, INC.
K063435	11/13/2006	GORE DUALMESH PLUS BIOMATERIAL GORE MYCROMESH PLUS BIOMATERIAL	W. L. GORE & ASSOCIATES, INC.
K053200	11/16/2005	GORE SEAMGUARD STAPLE LINE REINFORCEMENT MATERIAL	W.L. GORE & ASSOCIATES,INC
K053202	11/16/2005	GORE SEAMGUARD BIOABSORBABLE STAPLE LINE REINFORCEMENT MATERIAL	W.L. GORE & ASSOCIATES
K093934	12/22/2009	GORE HYBRID VASCULAR GRAFT	W.L. GORE & ASSOCIATES