Vein 360, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K232584Vein360 Reprocessed Visions PV.014P Rx Digital IVUS Catheter, Vein360 Reprocessed Eagle Eye PlatinumOctober 24, 2023
K230928Vein360 Reprocessed Visions PV.018 Digital IVUS CatheterAugust 25, 2023
K230584Vein360 Reprocessed Visions PV.035 Digital IVUS CatheterJune 6, 2023
K191073Vein360 Endovenous Radiofrequency Ablation (RFA) CatheterOctober 22, 2019