European Electronic Systems, Ltd.
Country not established
- Devices
- 1
What European Electronic Systems, Ltd. makes
European Electronic Systems, Ltd. manufactures the MK II TENS device, a transcutaneous electrical nerve stimulation (TENS) unit designed for pain management applications. This device delivers low-voltage electrical currents to the skin to alleviate acute or chronic pain through targeted nerve stimulation.
The MK II TENS falls under FDA Class II regulation and has been authorised via the 510(k) pathway. The company is based in the United States, and its devices are listed in the FDA’s 510(k) registry.
Catalogue
Model Mk Ii Tens Ref K833251
510(k) 510(k)
Frequently asked questions
How many devices does European Electronic Systems, Ltd. have in the registry?
The registry currently lists 1 device for European Electronic Systems, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list European Electronic Systems, Ltd.'s devices?
Among its 1 most recently registered device, European Electronic Systems, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do European Electronic Systems, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for European Electronic Systems, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from European Electronic Systems, Ltd. in the registry?
The most recently registered devices listed for European Electronic Systems, Ltd. include MODEL MK II TENS.