Neurozone Msh Incorporated
CanadaFDA applicant, unverified
- Devices
- 1
What Neurozone Msh Incorporated makes
Neurozone Msh Incorporated manufactures the Esprit Nova, a medical device designed for neurostimulation applications, likely targeting neurological or pain management therapies.
The Esprit Nova is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Esprit Nova Ref K182227
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neurozone Msh Incorporated have in the registry?
The registry currently lists 1 device for Neurozone Msh Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neurozone Msh Incorporated's devices?
Among its 1 most recently registered device, Neurozone Msh Incorporated has devices listed in FDA 510(k) (1 device).
What risk classes do Neurozone Msh Incorporated's devices fall under?
Among its 1 most recently registered device, the classes recorded for Neurozone Msh Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neurozone Msh Incorporated in the registry?
The most recently registered devices listed for Neurozone Msh Incorporated include Esprit Nova.