Akern USA, LLC
Country not established
- Devices
- 1
What Akern USA, LLC makes
Akern USA, LLC manufactures the Electrofluidgraph, a device used for measuring and analyzing bioelectrical impedance and fluid distribution within the body, often applied in clinical assessments of hydration status and body composition.
The Electrofluidgraph is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
Electrofluidgraph Ref K091369
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Akern USA, LLC have in the registry?
The registry currently lists 1 device for Akern USA, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Akern USA, LLC's devices?
Among its 1 most recently registered device, Akern USA, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Akern USA, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Akern USA, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Akern USA, LLC in the registry?
The most recently registered devices listed for Akern USA, LLC include ELECTROFLUIDGRAPH.