Inpromas
Country not established
- Devices
- 1
What Inpromas makes
Inpromas manufactures the OMNI-FIL, a medical device designed for filtration applications in healthcare settings, likely used in fluid management systems to remove particulate matter or contaminants.
The OMNI-FIL is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Omni-Fil Ref K863876
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Inpromas have in the registry?
The registry currently lists 1 device for Inpromas. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inpromas's devices?
Among its 1 most recently registered device, Inpromas has devices listed in FDA 510(k) (1 device).
What risk classes do Inpromas's devices fall under?
Among its 1 most recently registered device, the classes recorded for Inpromas's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inpromas in the registry?
The most recently registered devices listed for Inpromas include OMNI-FIL.