Arnet Optic Illusions
Country not established
- Devices
- 1
What Arnet Optic Illusions makes
Arnet Optic Illusions manufactures the ARNET and ARNETTE devices, which appear to be optical or vision-related products designed for specific diagnostic or therapeutic applications in ophthalmology.
These devices are classified as Class I under FDA regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Arnet Or Arnette Ref K960530
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arnet Optic Illusions have in the registry?
The registry currently lists 1 device for Arnet Optic Illusions. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arnet Optic Illusions's devices?
Among its 1 most recently registered device, Arnet Optic Illusions has devices listed in FDA 510(k) (1 device).
What risk classes do Arnet Optic Illusions's devices fall under?
Among its 1 most recently registered device, the classes recorded for Arnet Optic Illusions's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Arnet Optic Illusions in the registry?
The most recently registered devices listed for Arnet Optic Illusions include ARNET OR ARNETTE.