FDA 510(k) Applications Submitted by TODD KORNMANN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K020028	01/04/2002	6F MACH1/34356-XXX; 5F MACH1/35845-XXX; 7F MACH1/34357-XXX; 8F MACH1/34358-XXX	BOSTON SCIENTIFIC
K030645	02/28/2003	BOSTON SCIENTIFIC EXPRESS BILIARY LD UNMOUNTED STENT	BOSTON SCIENTIFIC CORP.
K010874	03/23/2001	6F MACH 1, MODEL 34356-XXX	BOSTON SCIENTIFIC CORP.
K021630	05/17/2002	BOSTON SCIENTIFIC EXPRESS BILIARY LD PREMOUNTED STENT SYSTEM	BOSTON SCIENTIFIC CORP.
K032360	07/31/2003	MODIFICATION TO BOSTON SCIENTIFIC EXPRESS BILIARY LD PREMOUNTED STENT SYSTEM AND EXPRESS BILIARY LD UNMOUNTED STENT	BOSTON SCIENTIFIC CORP.
K132578	08/16/2013	INTERLOCK - 18 FIBERED IDC OCCLUSION SYSTEM	BOSTON SCIENTIFIC CORP.
K012822	08/23/2001	MODIFICIATION TO: BILIARY WALLSTENT ENDOPROSTHEIS WITH MONORAIL DELIVERY SYSTEM, MODEL 71-XXX	BOSTON SCIENTIFIC SCIMED, INC.
K984062	11/16/1998	SEAL-AWAY HEMOSTASIS ADAPTER, MODEL 406229	DIAG CORP.
K024048	12/09/2002	MODIFICATION TO BOSTON SCIENTIFIC EXPRESS BILIARY LD PREMOUNTED STENT SYSTEM	BOSTON SCIENTIFIC SCIMED, INC.
K994334	12/23/1999	ULTRA-FLEX HEMOSTASIS INTRODUCER. MODEL 406XXX	DAIG CORP.