Class Class II

VXvue (K251410)

K251410 2025-11-04 Traditional
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Description

VXvue by Vieworks Co., Ltd., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251410
Clearance Date2025-11-04
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

Categories

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