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GuideLiner V3 Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172090
510(k) Type
Traditional
Applicant
Vascular Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2017
Days to Decision
101 days
Submission Type
Summary

GuideLiner V3 Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172090
510(k) Type
Traditional
Applicant
Vascular Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2017
Days to Decision
101 days
Submission Type
Summary