Last synced on 9 May 2025 at 11:05 pm

Vein360 Reprocessed Visions PV.014P Rx Digital IVUS Catheter, Vein360 Reprocessed Eagle Eye Platinum Rx Digital IVUS Catheter, Vein360 Reprocessed Eagle Eye Platinum ST Rx Digital IVUS Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232584
510(k) Type
Traditional
Applicant
Vein 360 LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2023
Days to Decision
60 days
Submission Type
Summary

Vein360 Reprocessed Visions PV.014P Rx Digital IVUS Catheter, Vein360 Reprocessed Eagle Eye Platinum Rx Digital IVUS Catheter, Vein360 Reprocessed Eagle Eye Platinum ST Rx Digital IVUS Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232584
510(k) Type
Traditional
Applicant
Vein 360 LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2023
Days to Decision
60 days
Submission Type
Summary