Class Class II

AIBOLIT 3D+ (K222458)

K222458 2023-01-12 Traditional
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Description

AIBOLIT 3D+ by Aibolit Technologies, LLC — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222458
Clearance Date2023-01-12
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

Categories

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