General Polymers
Country not established
- Devices
- 1
What General Polymers makes
General Polymers manufactures the Bousser’s Urinal, a disposable urinal designed for single-use medical or clinical applications.
The Bousser’s Urinal is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Bouser's Urinal Ref K970465
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does General Polymers have in the registry?
The registry currently lists 1 device for General Polymers. Devices recorded under merged duplicate company entries are counted once.
Which registries list General Polymers's devices?
Among its 1 most recently registered device, General Polymers has devices listed in FDA 510(k) (1 device).
What risk classes do General Polymers's devices fall under?
Among its 1 most recently registered device, the classes recorded for General Polymers's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from General Polymers in the registry?
The most recently registered devices listed for General Polymers include BOUSER'S URINAL.