Clearance Summary
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 received FDA 510(k) clearance under submission number K232584, sponsored by Vein 360, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2023-10-24.
- Submission: K232584
- Applicant / Sponsor: Vein 360, LLC
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1200
- Decision date: 2023-10-24
Classification & Regulation
This clearance is catalogued under FDA product code OWQ and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.