A C Cossor & Son (Surgical) Limited
United KingdomFDA 510(k) applicant, unverified
- Devices
- 1
Catalogue
Greenlight 300 Ref K040410
What A C Cossor & Son (Surgical) Limited makes
A C Cossor & Son (Surgical) Limited makes medical devices such as the GREENLIGHT 300, which is a specific type of product.
The company's portfolio is regulated as Class II devices and is listed in the fda_510k registry, with the company based in the US.
Frequently asked questions
How many devices does A C Cossor & Son (Surgical) Limited have in the registry?
The registry currently lists 1 device for A C Cossor & Son (Surgical) Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list A C Cossor & Son (Surgical) Limited's devices?
Among its 1 most recently registered device, A C Cossor & Son (Surgical) Limited has devices listed in FDA 510(k) (1 device).
What risk classes do A C Cossor & Son (Surgical) Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for A C Cossor & Son (Surgical) Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from A C Cossor & Son (Surgical) Limited in the registry?
The most recently registered devices listed for A C Cossor & Son (Surgical) Limited include GREENLIGHT 300.