Qure.Ai Technologies

Qure.Ai Technologies — FDA 510(k) Submissions

Qure.Ai Technologies has submitted 9 FDA 510(k) premarket notifications since 2020, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Automated Radiological Image Processing Software, Radiological Computer-assisted Triage And Notification Software, Analyzer, Medical Image, Radiological Computer-assisted Prioritization Software For Lesions . Use the specialty filter in the sidebar to narrow results.