Quibim S.L.

Quibim S.L. — FDA 510(k) Submissions

Quibim S.L. has submitted 3 FDA 510(k) premarket notifications since 2021, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Radiological Computer Assisted Detection/diagnosis Software For Lesions Suspicious For Cancer, System, Image Processing, Radiological, Automated Radiological Image Processing Software . Use the specialty filter in the sidebar to narrow results.