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Idev Technologies, Inc.

FDA 510(k) & PMA Approved Devices — 11 products

Total Devices11
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K130591 SUPERA VERITASFGE2013-05-02 View
510(k) K122546 SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEMFGE2012-12-07 View
510(k) K111627 SUPERA VERITAS(R) INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEMFGE2012-08-21 View
510(k) K111766 SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPTIC BILIARY SYSTEMSFGE2011-10-19 View
510(k) K093893 SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEMFGE2010-10-05 View
510(k) K071646 SUPERA INTERWOVEN SELF-EXPANDING BILIARY NITINOL STENT DELIVERY CATHETER, MODEL # S-04-040-120FGE2008-01-31 View
510(k) K060557 SURESAVE TM SELF-EXPANDABLE NITINOL STENT AND PRECISION TM DELIVERY CATHETER-SS06120060FGE2006-08-15 View
510(k) K050926 TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30120060MMX2005-05-09 View
510(k) K041374 AKONYA ELIMINATOR MECHANICAL THROMBECTOMY DEVICE, MODEL EL10060060QEW2005-03-02 View
510(k) K033188 TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050MMX2003-11-19 View
510(k) K030504 AKONYA ELIMINATOR MECHANICAL THROMBECTOMY DEVICE, MODEL EL 10060060MCW2003-09-16 View
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