Vein 360, LLC
FDA 510(k) medical device clearances.
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.