TRIUX? neo (NM27000N ); MEGreview (SW26241N-B)
May 2024
149d
Megin OY
1
Total
1
Cleared
0
Denied
Megin OY — FDA 510(k) Submissions
Megin OY has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Source Localization Software For Electroencephalograph Or Magnetoencephalograph . Use the specialty filter in the sidebar to narrow results.
1 devices