Vein 360, LLC
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories2
Latest Approval2023-10-24
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K232584 | 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 | OWQ | 2023-10-24 | View |
| 510(k) | K230928 | Vein360 Reprocessed Visions PV.018 Digital IVUS Catheter | OWQ | 2023-08-25 | View |
| 510(k) | K230584 | Vein360 Reprocessed Visions PV.035 Digital IVUS Catheter | OWQ | 2023-06-06 | View |
| 510(k) | K191073 | Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter | NUJ | 2019-10-22 | View |
No matching devices.