Prolira B.V.

Prolira B.V. — FDA 510(k) Submissions

Prolira B.V. has submitted 2 FDA 510(k) premarket notifications since 2023, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrode, Cutaneous, Neuropsychiatric Interpretative Electroencephalograph Assessment Aid . Use the specialty filter in the sidebar to narrow results.