Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Endologix, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K120212 AFX INTRODUCER SYSTEMDYB2012-02-09 View
510(k) K111747 ENDOLOGIX AFX INTRODUCER SYSTEMDYB2011-07-12 View
510(k) K110090 AFX INTRODUCER SYSTEMDYB2011-05-26 View
510(k) K080360 ENDOLOGIX VISIFLEX DUAL LUMEN CATHETERDQY2008-04-08 View
510(k) K991601 DUAL LUMEN CATHETER, MODEL DL-35-90DQY1999-10-28 View
↑