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
K232584 08/25/2023 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 Vein 360 LLC


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