Edu Kit, Ltd.
Country not established
- Devices
- 1
What Edu Kit, Ltd. makes
Edu Kit, Ltd. manufactures the TNS MK I Stimulator, a device designed for transcutaneous nerve stimulation (TNS) therapy.
The TNS MK I Stimulator is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway in the United States.
Catalogue
Tns Mk I Stimulator Ref K812612
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Edu Kit, Ltd. have in the registry?
The registry currently lists 1 device for Edu Kit, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Edu Kit, Ltd.'s devices?
Among its 1 most recently registered device, Edu Kit, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Edu Kit, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Edu Kit, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Edu Kit, Ltd. in the registry?
The most recently registered devices listed for Edu Kit, Ltd. include TNS MK I STIMULATOR.