Mskai
Country not established
- Devices
- 1
What Mskai makes
Mskai manufactures the MSKai device, a medical imaging system designed for cardiac and vascular applications, enabling real-time visualization and analysis of blood flow and cardiac structures.
The MSKai device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
MSKai Ref K240793
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mskai have in the registry?
The registry currently lists 1 device for Mskai. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mskai's devices?
Among its 1 most recently registered device, Mskai has devices listed in FDA 510(k) (1 device).
What risk classes do Mskai's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mskai's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mskai in the registry?
The most recently registered devices listed for Mskai include MSKai.