Medical Device Manufacturer · TW , Taipei

Clearmind Biomedical

3 submissions · 3 cleared · Since 2020
3
Total
3
Cleared
0
Denied

Clearmind Biomedical — FDA 510(k) Submissions

Clearmind Biomedical has submitted 3 FDA 510(k) premarket notifications since 2020, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Endoscope, Neurological . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
Filters
All3 Neurology 3