FDA 510(k) Applications Submitted by JANIS F TARANTO

FDA 510(k) Number	Submission Date	Device Name	Applicant
K130004	01/02/2013	ULTRAFLEX ESOPHAGEAL NG STENT SYSTEM	Boston Scientific Corporation
K110833	03/25/2011	CRE BALLOON DILATATION CATHETER	Boston Scientific Corporation
K091816	06/18/2009	ULTRAFLEX ESOPHAGEAL NG STENT SYSTEM	Boston Scientific Corporation
K112994	10/07/2011	CRE DITATATION BALLON	Boston Scientific Corporation
K120983	04/02/2012	ULTRAFLEX ESOPHAGEAL NG STENT SYSTEM	Boston Scientific Corporation
K121048	04/06/2012	ULTRAFLEX TRACHEOBRONCHIAL STENT SYSTEM- STERILE UNCOVERED	BOSTON SCIENTIFIC CORP.
K131700	06/11/2013	SENSATION SHORT THROW, CAPTIFLEX, CAPTIVATOR, CAPTIVATOR II, PROFILE, SINGLE-USE POLYPECTOMY SNARES	BOSTON SCIENTIFIC CORP.
K122924	09/24/2012	CRE FIXED WIRE BALLON DILATION CATHETER	BOSTON SCIENTIFIC CORP.
K133987	12/26/2013	CAPTIVATOR II,SINGLE-USE POLYPECTOMY SNARES	Boston Scientific Corporation