PathAI, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
PathAI, Inc. has 2 FDA 510(k) cleared medical devices. Based in Boston, US.
Latest FDA clearance: Jun 2025. Active since 2022. Primary specialty: Pathology.
Browse the FDA 510(k) cleared devices submitted by PathAI, Inc. Filter by specialty or product code using the sidebar.
1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
2 devices