Neuro42, Inc.
Country not established
- Devices
- 1
What Neuro42, Inc. makes
Neuro42, Inc. manufactures the neuro42 MRI System, a specialized magnetic resonance imaging device designed for advanced neuroimaging applications.
The neuro42 MRI System is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
neuro42 MRI System Ref K232644
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neuro42, Inc. have in the registry?
The registry currently lists 1 device for Neuro42, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neuro42, Inc.'s devices?
Among its 1 most recently registered device, Neuro42, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Neuro42, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neuro42, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neuro42, Inc. in the registry?
The most recently registered devices listed for Neuro42, Inc. include neuro42 MRI System.