Kjaya Medical, LLC
Country not established
- Devices
- 1
What Kjaya Medical, LLC makes
Kjaya Medical, LLC manufactures the VOLUMINA, a medical device designed for precise fluid measurement and monitoring in clinical settings.
The VOLUMINA is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Volumina Ref K081215
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kjaya Medical, LLC have in the registry?
The registry currently lists 1 device for Kjaya Medical, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kjaya Medical, LLC's devices?
Among its 1 most recently registered device, Kjaya Medical, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Kjaya Medical, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kjaya Medical, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kjaya Medical, LLC in the registry?
The most recently registered devices listed for Kjaya Medical, LLC include VOLUMINA.