FDA 510(k) Applications Submitted by Vein 360 LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230584 | 03/02/2023 | Vein360 Reprocessed Visions PV.035 Digital IVUS Catheter | Vein 360 LLC |
| K230928 | 04/03/2023 | Vein360 Reprocessed Visions PV.018 Digital IVUS Catheter | Vein 360 LLC |
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