Class Class II

uDR Arria & uDR Aris (K252000)

K252000 2025-11-26 Traditional
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Description

uDR Arria & uDR Aris by Shanghai United Imaging Healthcare Co., Ltd., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252000
Clearance Date2025-11-26
Clearance TypeTraditional
Product CodeKPR
Regulation Number892.1680

Categories

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