Vein 360, LLC - FDA 510(k) Cleared Devices
Recent clearances: 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, Vein360 Reprocessed Visions PV.018 Digital IVUS Catheter, Vein360 Reprocessed Visions PV.035 Digital IVUS Catheter
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vein 360, LLC General & Plastic Surgery ✕
1 devices