Neutro-Tronics
Country not established
- Devices
- 1
What Neutro-Tronics makes
Neutro-Tronics manufactures the NEUROTRON 100, a medical device designed for neuromodulation therapy, likely targeting conditions such as chronic pain or neurological disorders through electrical stimulation.
The NEUROTRON 100 is classified as a Class II device under FDA regulations and is listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Neurotron 100 Ref K833086
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neutro-Tronics have in the registry?
The registry currently lists 1 device for Neutro-Tronics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neutro-Tronics's devices?
Among its 1 most recently registered device, Neutro-Tronics has devices listed in FDA 510(k) (1 device).
What risk classes do Neutro-Tronics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Neutro-Tronics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neutro-Tronics in the registry?
The most recently registered devices listed for Neutro-Tronics include NEUROTRON 100.