Agar Ginosar Electronics
IsraelFDA applicant, unverified
- Devices
- 1
What Agar Ginosar Electronics makes
Agar Ginosar Electronics manufactures the AGARRELIEF 10, a transcutaneous electrical nerve stimulator (TENS) device designed for pain relief through low-voltage electrical stimulation.
The AGARRELIEF 10 is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Agar Ginosar Electronics have in the registry?
The registry currently lists 1 device for Agar Ginosar Electronics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Agar Ginosar Electronics's devices?
Among its 1 most recently registered device, Agar Ginosar Electronics has devices listed in FDA 510(k) (1 device).
What risk classes do Agar Ginosar Electronics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Agar Ginosar Electronics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Agar Ginosar Electronics in the registry?
The most recently registered devices listed for Agar Ginosar Electronics include AGARRELIEF 10 TRANSCUTANEOUS ELEC NERVE STIMULATOR.