Class Class II

AISight Dx (K243391)

K243391 2025-06-26 Traditional
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Description

AISight Dx by PathAI, Inc. — FDA 510(k) cleared pathology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK243391
Clearance Date2025-06-26
Clearance TypeTraditional
Product CodeQKQ
Regulation Number864.3700

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