Epitel, Inc.

Epitel, Inc. — FDA 510(k) Submissions

Epitel, Inc. has submitted 4 FDA 510(k) premarket notifications since 2021, of which 4 received clearance as substantially equivalent to a predicate device.

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