Usfilter
Country not established
- Devices
- 1
What Usfilter makes
Usfilter manufactures the Bicarbonate Mixing and Dispensing (BICARB) System, a device designed for automated preparation and administration of bicarbonate solutions in medical settings.
The BICARB System is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Usfilter have in the registry?
The registry currently lists 1 device for Usfilter. Devices recorded under merged duplicate company entries are counted once.
Which registries list Usfilter's devices?
Among its 1 most recently registered device, Usfilter has devices listed in FDA 510(k) (1 device).
What risk classes do Usfilter's devices fall under?
Among its 1 most recently registered device, the classes recorded for Usfilter's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Usfilter in the registry?
The most recently registered devices listed for Usfilter include USFILTER BICARBONATE MIXING AND DISPENSING (BICARB) SYSTEM.