Vein 360, LLC
Vein 360, LLC holds FDA 510(k) medical device clearances, first cleared 2019, most recent 2023.
Top product codes for Vein 360, LLC
Recent clearances by Vein 360, LLC
- 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
- K230928 — Vein360 Reprocessed Visions PV.018 Digital IVUS Catheter
- K230584 — Vein360 Reprocessed Visions PV.035 Digital IVUS Catheter
- K191073 — Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter
Data sourced from openFDA. This site is unofficial and independent of the FDA.