Last synced on 25 April 2025 at 11:05 pm

Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191073
510(k) Type
Traditional
Applicant
Vein360, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2019
Days to Decision
183 days
Submission Type
Summary

Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191073
510(k) Type
Traditional
Applicant
Vein360, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2019
Days to Decision
183 days
Submission Type
Summary