Medical Device Manufacturer · IT , Abano Terme, Padova

Neurosoft , Ltd.

3 submissions · 3 cleared · Since 2015
3
Total
3
Cleared
0
Denied

Neurosoft , Ltd. — FDA 510(k) Submissions

Neurosoft , Ltd. has submitted 3 FDA 510(k) premarket notifications since 2015, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Non-normalizing Quantitative Electroencephalograph Software, Stimulator, Electrical, Evoked Response . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
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All3 Neurology 3