Elite Electromedical
Country not established
- Devices
- 1
What Elite Electromedical makes
Elite Electromedical manufactures the ELITE ELECTROMED L.I.T.E. 4/1, a medical device designed for electromedical therapy applications, likely including neuromuscular electrical stimulation or transcutaneous electrical nerve stimulation (TENS).
The device falls under FDA Class II regulation and is listed via the 510(k) pathway in the United States. The manufacturer is based in the US.
Catalogue
Elite Electromed L.I.T.E. 4/1 Ref K053507
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Elite Electromedical have in the registry?
The registry currently lists 1 device for Elite Electromedical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Elite Electromedical's devices?
Among its 1 most recently registered device, Elite Electromedical has devices listed in FDA 510(k) (1 device).
What risk classes do Elite Electromedical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Elite Electromedical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Elite Electromedical in the registry?
The most recently registered devices listed for Elite Electromedical include ELITE ELECTROMED L.I.T.E. 4/1.