FDA 510(k) Applications Submitted by Joni Creal

FDA 510(k) Number	Submission Date	Device Name	Applicant
K130366	02/13/2013	BARD DENALI FILTER SYSTEM- FEMORAL DELIVERY KIT AND JUGULAR DELIVERY KIT	C.R. BARD, INC.
K101431	05/21/2010	ECLIPSE FILTER SYSTEM-FEMORAL AND JUGULAR/SUBCLAVIAN DELIVERY KITS	C.R. BARD, INC.
K152136	07/31/2015	Recovery Cone Removal System	C.R. Bard, Inc.
K112497	08/29/2011	MERIDIAN FILTER SYSTEM - FEMORAL DELIVERY KIT	C.R. BARD, INC.
K102511	09/01/2010	MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT	C.R. BARD, INC.
K093659	11/25/2009	ECLIPSE FILTER SYSTEM-FEMORAL DELIVERY KIT, ECLIPSE FILTER SYSTEM-JUGULAR/SUBCLAVIAN DELIVERY KIT MODEL RF500F MODEL RF5	C.R. BARD, INC.