Morrison Center
Country not established
- Devices
- 1
What Morrison Center makes
The Morrison Center manufactures spectacle frames, including the Morrison Frame, designed for eyewear applications.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Morrison Frame, Spectacle Ref K940853
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Morrison Center have in the registry?
The registry currently lists 1 device for Morrison Center. Devices recorded under merged duplicate company entries are counted once.
Which registries list Morrison Center's devices?
Among its 1 most recently registered device, Morrison Center has devices listed in FDA 510(k) (1 device).
What risk classes do Morrison Center's devices fall under?
Among its 1 most recently registered device, the classes recorded for Morrison Center's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Morrison Center in the registry?
The most recently registered devices listed for Morrison Center include MORRISON FRAME, SPECTACLE.