Class Class II

Vein360 Reprocessed Visions PV.035 Digital IVUS Catheter (K230584)

K230584 2023-06-06 Traditional
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Description

Vein360 Reprocessed Visions PV.035 Digital IVUS Catheter by Vein 360, LLC — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230584
Clearance Date2023-06-06
Clearance TypeTraditional
Product CodeOWQ
Regulation Number870.1200

Categories

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