Cillus Company, Inc.
Country not established
- Devices
- 1
What Cillus Company, Inc. makes
Cillus Company, Inc. manufactures the Brillette Model, a Class I medical device designed for a specific clinical application (device category unspecified in provided data).
The Brillette Model is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Brillette Model Ref K842835
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cillus Company, Inc. have in the registry?
The registry currently lists 1 device for Cillus Company, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cillus Company, Inc.'s devices?
Among its 1 most recently registered device, Cillus Company, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cillus Company, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cillus Company, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Cillus Company, Inc. in the registry?
The most recently registered devices listed for Cillus Company, Inc. include BRILLETTE MODEL.