Brooke Intl.
Country not established
- Devices
- 1
What Brooke Intl. makes
Brooke International manufactures the Cytosmear Brush, a diagnostic device used for collecting cellular samples from mucosal surfaces, such as the cervix or gastrointestinal tract, for cytological examination.
The Cytosmear Brush is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Cytosmear Brush Ref K904160
510(k) 510(k)
Frequently asked questions
How many devices does Brooke Intl. have in the registry?
The registry currently lists 1 device for Brooke Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Brooke Intl.'s devices?
Among its 1 most recently registered device, Brooke Intl. has devices listed in FDA 510(k) (1 device).
What risk classes do Brooke Intl.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Brooke Intl.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Brooke Intl. in the registry?
The most recently registered devices listed for Brooke Intl. include CYTOSMEAR BRUSH.