Neurovision, Inc.
Country not established
- Devices
- 1
What Neurovision, Inc. makes
Neurovision, Inc. manufactures the AA-1 System, a medical device designed for neurovisual diagnostics and assessment, likely used in evaluating eye movement and binocular vision function.
The AA-1 System is classified as a Class I device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Aa-1 System Ref K012530
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neurovision, Inc. have in the registry?
The registry currently lists 1 device for Neurovision, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neurovision, Inc.'s devices?
Among its 1 most recently registered device, Neurovision, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Neurovision, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neurovision, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Neurovision, Inc. in the registry?
The most recently registered devices listed for Neurovision, Inc. include AA-1 SYSTEM.