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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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