Class Class II

AccuCheck (K250696)

K250696 2025-10-24 Traditional
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Description

AccuCheck by Manteia Technologies Co., Ltd., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250696
Clearance Date2025-10-24
Clearance TypeTraditional
Product CodeIYE
Regulation Number892.5050

Categories

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