Vein 360, LLC
Vein 360, LLC appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 24, 2023.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K232584 | Vein360 Reprocessed Visions PV.014P Rx Digital IVUS Catheter, Vein360 Reprocessed Eagle Eye Platinum | October 24, 2023 |
| K230928 | Vein360 Reprocessed Visions PV.018 Digital IVUS Catheter | August 25, 2023 |
| K230584 | Vein360 Reprocessed Visions PV.035 Digital IVUS Catheter | June 6, 2023 |
| K191073 | Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter | October 22, 2019 |