Ferrania USA, Inc.
Country not established
- Devices
- 1
What Ferrania USA, Inc. makes
Ferrania USA, Inc. manufactures mammography cassettes, including the LIFERAY FW and LIFERAY KW models, designed for digital and film-based breast imaging systems.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ferrania USA, Inc. have in the registry?
The registry currently lists 1 device for Ferrania USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ferrania USA, Inc.'s devices?
Among its 1 most recently registered device, Ferrania USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ferrania USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ferrania USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ferrania USA, Inc. in the registry?
The most recently registered devices listed for Ferrania USA, Inc. include LIFERAY FW MAMMO CASSETTE, LIFERAY KW MAMMO CASETTE.