Uab Research Foundation
Country not established
- Devices
- 1
What Uab Research Foundation makes
The Uab Research Foundation manufactures the Bedside Fluid Management System 1000 (FMS-1000), a device designed for monitoring and managing intravenous fluid administration in clinical settings.
The FMS-1000 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
Bedside Fluid Management System 1000 (Fms-1000) Ref K910323
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Uab Research Foundation have in the registry?
The registry currently lists 1 device for Uab Research Foundation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Uab Research Foundation's devices?
Among its 1 most recently registered device, Uab Research Foundation has devices listed in FDA 510(k) (1 device).
What risk classes do Uab Research Foundation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Uab Research Foundation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Uab Research Foundation in the registry?
The most recently registered devices listed for Uab Research Foundation include BEDSIDE FLUID MANAGEMENT SYSTEM 1000 (FMS-1000).