Class Class II

PreXion3D Expedition (K222150)

K222150 2023-01-12 Traditional
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Description

PreXion3D Expedition by Prexion Corporation — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222150
Clearance Date2023-01-12
Clearance TypeTraditional
Product CodeOAS
Regulation Number892.1750

Categories

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