FDA 510(k) Applications Submitted by IDEV TECHNOLOGIES, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K111766 06/23/2011 SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPTIC BILIARY SYSTEMS IDEV TECHNOLOGIES, INC.
K130591 03/07/2013 SUPERA VERITAS IDEV TECHNOLOGIES, INC.
K111627 06/10/2011 SUPERA VERITAS(R) INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM IDEV TECHNOLOGIES, INC.
K122546 08/21/2012 SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM IDEV TECHNOLOGIES, INC.
K093893 12/18/2009 SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM IDEV TECHNOLOGIES, INC.
K030504 02/19/2003 AKONYA ELIMINATOR MECHANICAL THROMBECTOMY DEVICE, MODEL EL 10060060 IDEV TECHNOLOGIES, INC.
K041374 05/24/2004 AKONYA ELIMINATOR MECHANICAL THROMBECTOMY DEVICE, MODEL EL10060060 IDEV TECHNOLOGIES, INC.
K033188 10/01/2003 TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050 IDEV TECHNOLOGIES, INC.
K050926 04/13/2005 TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060 IDEV TECHNOLOGIES, INC.
K060557 03/02/2006 SURESAVE TM SELF-EXPANDABLE NITINOL STENT AND PRECISION TM DELIVERY CATHETER-SS06120060 IDEV TECHNOLOGIES, INC.
K071646 06/18/2007 SUPERA INTERWOVEN SELF-EXPANDING BILIARY NITINOL STENT DELIVERY CATHETER, MODEL # S-04-040-120 IDEV TECHNOLOGIES, INC.


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