FDA 510(k) Applications Submitted by JANE BEGGS

FDA 510(k) Number	Submission Date	Device Name	Applicant
DEN130007	02/19/2013	AXIOS STENT AND DELIVERY SYSTEM	XLUMENA, INC
K140561	03/05/2014	AXIOS STENT AND DELIVERY SYSTEM (WITH 10MM X 10MM STENT) AXIOS STENT AND DELIVERY SYSTEM (WITH 15MM X 10MM STENT)	XLUMENA, INC.
K001371	05/01/2000	CARDEON ASCENDING BALLOON CANNULA (ABC)	CARDEON CORP.
K022042	06/24/2002	MODIFICATION TO CARDEON ASCENDING BALLOON CANNULA (ABC)	CARDEON CORP.
K022174	07/03/2002	MODIFICATION TO CARDEON AEGIS CATHETER	CARDEON CORP.
K042156	08/10/2004	CARDEON COBRA CATHETER	CARDEON CORP.
K013593	10/30/2001	CARDEON AEGIS CATHETER	CARDEON CORP.
K024058	12/09/2002	MODIFICATION TO CARDEON AEGIS CATHETER	CARDEON CORP.