Strohl Medical Technologies
Country not established
- Devices
- 1
What Strohl Medical Technologies makes
Strohl Medical Technologies manufactures the NEUROEPG System, a device designed for electrophysiological monitoring and stimulation in neurosurgical procedures, particularly for epilepsy patient evaluation.
The NEUROEPG System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Neuroepg System Ref K123843
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Strohl Medical Technologies have in the registry?
The registry currently lists 1 device for Strohl Medical Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Strohl Medical Technologies's devices?
Among its 1 most recently registered device, Strohl Medical Technologies has devices listed in FDA 510(k) (1 device).
What risk classes do Strohl Medical Technologies's devices fall under?
Among its 1 most recently registered device, the classes recorded for Strohl Medical Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Strohl Medical Technologies in the registry?
The most recently registered devices listed for Strohl Medical Technologies include NEUROEPG SYSTEM.