Apollo Fluid Dynamics
Country not established
- Devices
- 1
What Apollo Fluid Dynamics makes
Apollo Fluid Dynamics manufactures the Apollo Air Fluidized Bed, a device designed for fluidized bed therapy to support wound care and skin integrity management.
The Apollo Air Fluidized Bed is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Apollo Air Fluidized Bed Ref K842987
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Apollo Fluid Dynamics have in the registry?
The registry currently lists 1 device for Apollo Fluid Dynamics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Apollo Fluid Dynamics's devices?
Among its 1 most recently registered device, Apollo Fluid Dynamics has devices listed in FDA 510(k) (1 device).
What risk classes do Apollo Fluid Dynamics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Apollo Fluid Dynamics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Apollo Fluid Dynamics in the registry?
The most recently registered devices listed for Apollo Fluid Dynamics include APOLLO AIR FLUIDIZED BED.