Alvar
Country not established
- Devices
- 1
What Alvar makes
Alvar develops electrodiagnostic systems for brain mapping, including the CARTOVAR platform, which supports intraoperative and preoperative neurological mapping to guide surgical procedures.
The company’s products are classified as Class II medical devices under FDA regulations and are authorised via the 510(k) pathway. Alvar is based in the United States.
Catalogue
Cartovar Brain Mapping Electrodiagnostics Ref K853420
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alvar have in the registry?
The registry currently lists 1 device for Alvar. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alvar's devices?
Among its 1 most recently registered device, Alvar has devices listed in FDA 510(k) (1 device).
What risk classes do Alvar's devices fall under?
Among its 1 most recently registered device, the classes recorded for Alvar's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alvar in the registry?
The most recently registered devices listed for Alvar include CARTOVAR BRAIN MAPPING ELECTRODIAGNOSTICS.