REMI Remote EEG Monitoring System
Mar 2025
172d
Epitel
1
Total
1
Cleared
0
Denied
Epitel — FDA 510(k) Submissions
Epitel has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Reduced- Montage Standard Electroencephalograph . Use the specialty filter in the sidebar to narrow results.
1 devices