Medical Device Manufacturer · US , Eden Prairie , MN

Neuroone Medical Technologies Corp.

4 submissions · 4 cleared · Since 2021
4
Total
4
Cleared
0
Denied

Neuroone Medical Technologies Corp. — FDA 510(k) Submissions

Neuroone Medical Technologies Corp. 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 Electrode, Depth, Generator, Lesion, Radiofrequency, Probe, Radiofrequency Lesion . Use the specialty filter in the sidebar to narrow results.

4 devices
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All4 Neurology 4