Translational MRI, LLC
Country not established
- Devices
- 1
What Translational MRI, LLC makes
Translational Mri, LLC makes the CereFlow V1.2 device.
The CereFlow V1.2 is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
CereFlow™ V1.2 Ref K211059
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Translational Mri, LLC have in the registry?
The registry currently lists 1 device for Translational Mri, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Translational Mri, LLC's devices?
Among its 1 most recently registered device, Translational Mri, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Translational Mri, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Translational Mri, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Translational Mri, LLC in the registry?
The most recently registered devices listed for Translational Mri, LLC include CereFlow™ V1.2.