Holberg Eeg AS

Holberg Eeg AS — FDA 510(k) Submissions

Holberg Eeg AS has submitted 2 FDA 510(k) premarket notifications since 2024, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Automatic Event Detection Software For Full-montage Electroencephalograph . Use the specialty filter in the sidebar to narrow results.