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Lumend, Inc.

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

Total Devices11
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K043534 MODIFICATION TO OUTBACK CATHETERDQY2005-01-21 View
510(k) K040771 MODIFICATION TO OUTBACK CATHETERDQY2004-04-23 View
510(k) K033535 LUMEND FRONTRUNNER CTO CATHETER AND ACCESSORIESPDU2004-01-07 View
510(k) K032298 MODIFICATION TO OUTBACK CATHETERDQY2003-08-26 View
510(k) K031005 LUMEND FRONTRUNNER GW CTO CATHETERPDU2003-06-18 View
510(k) K023114 LUMEND FRONTRUNNER CTO CATHETERPDU2003-01-23 View
510(k) K023223 MODIFICATION TO LUMEND FRONTRUNNER CTO CATHETERDQY2002-10-24 View
510(k) K013284 LUMEND FRONTRUNNER CTO CORONARY CATHETERDQY2002-02-11 View
510(k) K011562 LUMEND PERCUTANEOUS CATHETERDQY2002-01-16 View
510(k) K014117 MODIFICATION TO OUTBACK CATHETERDQY2002-01-11 View
510(k) K001577 OUTBACK CATHETERDQY2001-01-11 View
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