FDA 510(k) Applications Submitted by JOSEPH C GRIFFIN, III

FDA 510(k) Number	Submission Date	Device Name	Applicant
K961513	04/19/1996	PROCATH LOCKING PEEL-AWAY INTRODUCER/PEEL-AWAY INTRODUCER SET	EP MEDSYSTEMS
K081996	07/14/2008	FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM	FLEXIBLE STENTING SOLUTIONS, INC.
K120452	02/14/2012	FLEXSTENT BILIARY SELF-EXPANDING STENT SYSTEM	FLEXIBLE STENTING SOLUTIONS, INC.
K121125	04/13/2012	FLEXSTENT BILIARY SELF-EXPANDING STENT SYSTEM	FLEXIBLE STENTING SOLUTIONS, INC.
K112522	08/31/2011	FLEXSTENT BILIARY SELF-EXPANDING STENT SYSTEM	FLEXIBLE STENTING SOLUTIONS, INC.
K994011	11/26/1999	EP MEDSYSTEMS, EP-WORKMATE	EP MEDSYSTEMS, INC.
K991001	03/25/1999	MODIFICATION OF PROCATH ELECTROPHYSIOLOGY CATHETER, EP MEDSYSTEMS ELECTROPHYSIOLOGY CATHETER	EP MEDSYSTEMS
K102519	09/02/2010	FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM MODEL FLX-DDLLL-BX	FLEXIBLE STENTING SOLUTIONS, INC.
K984150	11/19/1998	PROCATH ELECTROPHYSIOLOGY CATHETER, EP MEDSYSTEMS ELECTROPHYSIOLOGY CATHETER	EP MEDSYSTEMS