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GUIDELINER V2 CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112082
510(k) Type
Special
Applicant
Vascular Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2011
Days to Decision
133 days
Submission Type
Summary

GUIDELINER V2 CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112082
510(k) Type
Special
Applicant
Vascular Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2011
Days to Decision
133 days
Submission Type
Summary