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ENDOLOGIX VISIFLEX DUAL LUMEN CATHETER

Page Type
Cleared 510(K)
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)
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