Class Class II

InferOperate Suite (K250237)

K250237 2025-09-15 Traditional
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Description

InferOperate Suite by Beijing Infervision Healthcare Medical Technology Co., Ltd., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250237
Clearance Date2025-09-15
Clearance TypeTraditional
Product CodeQIH
Regulation Number892.2050

Categories

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