Mobilemedtek
Country not established
- Devices
- 1
What Mobilemedtek makes
Mobilemedtek manufactures the ElectroTek, a medical device designed for electrodiagnostic testing, including nerve conduction studies and electromyography (EMG).
The ElectroTek is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
ElectroTek Ref K170441
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mobilemedtek have in the registry?
The registry currently lists 1 device for Mobilemedtek. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mobilemedtek's devices?
Among its 1 most recently registered device, Mobilemedtek has devices listed in FDA 510(k) (1 device).
What risk classes do Mobilemedtek's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mobilemedtek's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mobilemedtek in the registry?
The most recently registered devices listed for Mobilemedtek include ElectroTek.