Medical Device Manufacturer · DE , Munich

Mag & More GmbH

4 submissions · 4 cleared · Since 2018
4
Total
4
Cleared
0
Denied

Mag & More GmbH — FDA 510(k) Submissions

Mag & More GmbH has submitted 4 FDA 510(k) premarket notifications since 2018, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Transcranial Magnetic Stimulator . Use the specialty filter in the sidebar to narrow results.

4 devices
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All4 Neurology 4