Beacon Biosignals, Inc.

Beacon Biosignals, Inc. — FDA 510(k) Submissions

Beacon Biosignals, Inc. has submitted 3 FDA 510(k) premarket notifications since 2023, of which 3 received clearance as substantially equivalent to a predicate device.

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