Rijuven Corp
Country not established
- Devices
- 1
What Rijuven Corp makes
Rijuven Corp manufactures the Cardiosleeve, a medical device designed for cardiac monitoring and diagnostic purposes, likely used in electrophysiological studies or arrhythmia detection.
The Cardiosleeve is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Cardiosleeve Ref K131287
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rijuven Corp have in the registry?
The registry currently lists 1 device for Rijuven Corp. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rijuven Corp's devices?
Among its 1 most recently registered device, Rijuven Corp has devices listed in FDA 510(k) (1 device).
What risk classes do Rijuven Corp's devices fall under?
Among its 1 most recently registered device, the classes recorded for Rijuven Corp's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rijuven Corp in the registry?
The most recently registered devices listed for Rijuven Corp include CARDIOSLEEVE.