Medical Device Manufacturer · AT , Schiedlberg

G.Tec Medical Engineering GmbH

6 submissions · 6 cleared · Since 2006
6
Total
6
Cleared
0
Denied

G.Tec Medical Engineering GmbH — FDA 510(k) Submissions

G.Tec Medical Engineering GmbH has submitted 6 FDA 510(k) premarket notifications since 2006, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Amplifier, Physiological Signal, Electrode, Cortical, Normalizing Quantitative Electroencephalograph Software, Stimulator, Muscle, Powered . Use the specialty filter in the sidebar to narrow results.

6 devices
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All6 Neurology 5 Physical Medicine 1