Canadian Medical Brush, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Canadian Medical Brush, Inc. makes
Canadian Medical Brush, Inc. manufactures the Cervical Cytology C-Brush Model CMB-1010, a device designed for collecting cervical cell samples during gynecological examinations.
The company’s product portfolio is regulated under FDA’s Class II device classification and requires 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Cervical Cytology C-Brush Model Cmb-1010 Ref K980356
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Canadian Medical Brush, Inc. have in the registry?
The registry currently lists 1 device for Canadian Medical Brush, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Canadian Medical Brush, Inc.'s devices?
Among its 1 most recently registered device, Canadian Medical Brush, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Canadian Medical Brush, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Canadian Medical Brush, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Canadian Medical Brush, Inc. in the registry?
The most recently registered devices listed for Canadian Medical Brush, Inc. include CERVICAL CYTOLOGY C-BRUSH MODEL CMB-1010.