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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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