Class Class II

BONX805 (K243864)

K243864 2025-09-12 Traditional
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Description

BONX805 by Bontech Co., Ltd., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK243864
Clearance Date2025-09-12
Clearance TypeTraditional
Product CodeIZL
Regulation Number892.1720

Categories

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