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

FDA 510(k) Number Submission Date Device Name Applicant
K960803 02/27/1996 RX TEXTILES STERILE STOCKINETTE RX TEXTILES, 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
K050957 04/15/2005 EUTROCHAR SPECIAL DEVICES, INC.


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