Eletromed, Inc.
Country not established
- Devices
- 1
What Eletromed, Inc. makes
Eletromed, Inc. manufactures reusable neurostimulation electrodes.
The company is based in the United States, and its products are classified as Class II medical devices that are listed in the FDA 510(k) registry.
Catalogue
Electromed Reusable Neurostimulation Electrodes Ref K030800
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eletromed, Inc. have in the registry?
The registry currently lists 1 device for Eletromed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eletromed, Inc.'s devices?
Among its 1 most recently registered device, Eletromed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Eletromed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Eletromed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eletromed, Inc. in the registry?
The most recently registered devices listed for Eletromed, Inc. include ELECTROMED REUSABLE NEUROSTIMULATION ELECTRODES.