Vital Art and Science Incorporated
United StatesFDA applicant, unverified
- Devices
- 2
What Vital Art and Science Incorporated makes
Vital Art and Science Incorporated manufactures the myVision Track Model 005, a device branded as MYVISIONTRACK™, designed for monitoring and tracking visual function or eye movement in clinical or research settings.
The company’s portfolio is regulated under FDA Class I devices and is listed in the 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
myVision Track Model 005 Ref K143211
Regimes: 510(k) Registry: 510(k)Myvisiontrack(Tm) Ref K121738
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vital Art and Science Incorporated have in the registry?
The registry currently lists 2 devices for Vital Art and Science Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vital Art and Science Incorporated's devices?
Among its 2 most recently registered devices, Vital Art and Science Incorporated has devices listed in FDA 510(k) (2 devices).
What risk classes do Vital Art and Science Incorporated's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Vital Art and Science Incorporated's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Vital Art and Science Incorporated in the registry?
The most recently registered devices listed for Vital Art and Science Incorporated include myVision Track Model 005 and MYVISIONTRACK(TM).