Endologix, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Endologix, Inc. Cardiovascular ✕
5 devices
Cleared
Feb 09, 2012
AFX INTRODUCER SYSTEM
Cardiovascular
16d
Cleared
Jul 12, 2011
ENDOLOGIX AFX INTRODUCER SYSTEM
Cardiovascular
20d
Cleared
May 26, 2011
AFX INTRODUCER SYSTEM
Cardiovascular
134d
Cleared
Apr 08, 2008
ENDOLOGIX VISIFLEX DUAL LUMEN CATHETER
Cardiovascular
57d
Cleared
Oct 28, 1999
DUAL LUMEN CATHETER, MODEL DL-35-90
Cardiovascular
171d