Western Systems, Inc.
Country not established
- Devices
- 1
What Western Systems, Inc. makes
Western Systems, Inc. manufactures the AIR ALIVE device, which appears to be a Class II medical product designed for air purification or ventilation applications, likely targeting indoor air quality solutions.
The AIR ALIVE device is regulated under the US FDA as a Class II product, requiring a 510(k) clearance. It is listed in the FDA’s 510(k) database, and the company is based in the United States.
Catalogue
Air Alive Ref K812320
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Western Systems, Inc. have in the registry?
The registry currently lists 1 device for Western Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Western Systems, Inc.'s devices?
Among its 1 most recently registered device, Western Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Western Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Western Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Western Systems, Inc. in the registry?
The most recently registered devices listed for Western Systems, Inc. include AIR ALIVE.