Medical Device Manufacturer · US , Boston , MA

PathAI, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2022
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - PathAI, Inc. Pathology ✕
2 devices
1-2 of 2
Cleared Jun 26, 2025
AISight Dx
K243391 · QKQ
Pathology · 238d
Cleared Aug 11, 2022
Novo
K212361 · QKQ
Pathology · 377d
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