FDA 510(k) Applications Submitted by ENDOLOGIX, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K080360 02/11/2008 ENDOLOGIX VISIFLEX DUAL LUMEN CATHETER ENDOLOGIX, INC.
K110090 01/12/2011 AFX INTRODUCER SYSTEM ENDOLOGIX, INC.
K120212 01/24/2012 AFX INTRODUCER SYSTEM ENDOLOGIX, INC.
K111747 06/22/2011 ENDOLOGIX AFX INTRODUCER SYSTEM ENDOLOGIX, INC.
K991601 05/10/1999 DUAL LUMEN CATHETER, MODEL DL-35-90 ENDOLOGIX, INC.


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