Last synced on 25 January 2026 at 3:41 am

ENDOLOGIX VISIFLEX DUAL LUMEN CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080360
510(k) Type
Special
Applicant
Endologix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/2008
Days to Decision
57 days
Submission Type
Summary

ENDOLOGIX VISIFLEX DUAL LUMEN CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080360
510(k) Type
Special
Applicant
Endologix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/2008
Days to Decision
57 days
Submission Type
Summary