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GORE® Tri-Lobe Balloon Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250410
510(k) Type
Traditional
Applicant
W. L. Gore & Associates, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2025
Days to Decision
109 days
Submission Type
Summary

GORE® Tri-Lobe Balloon Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250410
510(k) Type
Traditional
Applicant
W. L. Gore & Associates, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2025
Days to Decision
109 days
Submission Type
Summary