Avicenna.Ai

Avicenna.Ai — FDA 510(k) Submissions

Avicenna.Ai has submitted 7 FDA 510(k) premarket notifications since 2020, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Radiological Computer-assisted Triage And Notification Software, Computer-assisted Diagnostic Software For Lesions Suspicious For Cancer, Radiological Computer-assisted Prioritization Software For Lesions . Use the specialty filter in the sidebar to narrow results.