Amana Medical Group
Country not established
- Devices
- 1
What Amana Medical Group makes
Amana Medical Group manufactures electrotherapeutic devices, including the Modified Amana Electotherapeutic System, designed for therapeutic electrical stimulation applications.
The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Modified Amana Electrotherapeutic System Ref K875072
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Amana Medical Group have in the registry?
The registry currently lists 1 device for Amana Medical Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amana Medical Group's devices?
Among its 1 most recently registered device, Amana Medical Group has devices listed in FDA 510(k) (1 device).
What risk classes do Amana Medical Group's devices fall under?
Among its 1 most recently registered device, the classes recorded for Amana Medical Group's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Amana Medical Group in the registry?
The most recently registered devices listed for Amana Medical Group include MODIFIED AMANA ELECTROTHERAPEUTIC SYSTEM.