Neurocare Group
Country not established
- Devices
- 1
What Neurocare Group makes
Neurocare Group manufactures cerebrospinal fluid (CSF) shunt valves, including the GEMINI Standard and Mini models, designed for managing hydrocephalus in pediatric and adult patients by regulating CSF flow within the ventricular system.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The company operates from the United States.
Catalogue
Gemini Standard And Mini Valves Ref K974708
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neurocare Group have in the registry?
The registry currently lists 1 device for Neurocare Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neurocare Group's devices?
Among its 1 most recently registered device, Neurocare Group has devices listed in FDA 510(k) (1 device).
What risk classes do Neurocare Group's devices fall under?
Among its 1 most recently registered device, the classes recorded for Neurocare Group's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neurocare Group in the registry?
The most recently registered devices listed for Neurocare Group include GEMINI STANDARD AND MINI VALVES.