Neurotek, Inc.
Country not established
- Devices
- 1
What Neurotek, Inc. makes
Neurotek, Inc. manufactures the NTI-1000, a device designed for neurostimulation or neuromodulation applications, likely targeting specific neurological or musculoskeletal conditions.
The NTI-1000 is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Nti-1000 Ref K894097
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neurotek, Inc. have in the registry?
The registry currently lists 1 device for Neurotek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neurotek, Inc.'s devices?
Among its 1 most recently registered device, Neurotek, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Neurotek, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neurotek, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neurotek, Inc. in the registry?
The most recently registered devices listed for Neurotek, Inc. include NTI-1000.