General Electrical Espanola, S.A.
Country not established
- Devices
- 1
What General Electrical Espanola, S.A. makes
General Electrical Española, S.A. manufactures the Televix, a medical device designed for diagnostic or therapeutic use within its specified category.
The Televix is classified as a Class II device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Televix Ref K790692
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does General Electrical Espanola, S.A. have in the registry?
The registry currently lists 1 device for General Electrical Espanola, S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list General Electrical Espanola, S.A.'s devices?
Among its 1 most recently registered device, General Electrical Espanola, S.A. has devices listed in FDA 510(k) (1 device).
What risk classes do General Electrical Espanola, S.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for General Electrical Espanola, S.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from General Electrical Espanola, S.A. in the registry?
The most recently registered devices listed for General Electrical Espanola, S.A. include TELEVIX.