Vein 360, LLC
4 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| 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 (K232584) | Vein 360, LLC | 2023-10-24 |
| Vein360 Reprocessed Visions PV.018 Digital IVUS Catheter (K230928) | Vein 360, LLC | 2023-08-25 |
| Vein360 Reprocessed Visions PV.035 Digital IVUS Catheter (K230584) | Vein 360, LLC | 2023-06-06 |
| Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter (K191073) | Vein 360, LLC | 2019-10-22 |
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Every clearance here is in the API, with alerts when new ones post.