Revue Intl.
Country not established
- Devices
- 1
What Revue Intl. makes
Revue Intl. manufactures the Augusta Valentini device.
The Augusta Valentini is a Class I medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Augusta Valentini Ref K923884
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Revue Intl. have in the registry?
The registry currently lists 1 device for Revue Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Revue Intl.'s devices?
Among its 1 most recently registered device, Revue Intl. has devices listed in FDA 510(k) (1 device).
What risk classes do Revue Intl.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Revue Intl.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Revue Intl. in the registry?
The most recently registered devices listed for Revue Intl. include AUGUSTA VALENTINI.