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FDA 510(k) Applications Submitted by JOSEPH C GRIFFIN
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
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