Class Class II

PerfusionGo Plus (K221627)

K221627 2023-01-19 Traditional
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Description

PerfusionGo Plus by Yukun (Beijing) Technology Co., Ltd. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK221627
Clearance Date2023-01-19
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

Categories

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