The Western Diagnostics Co.
Country not established
- Devices
- 1
What The Western Diagnostics Co. makes
The Western Diagnostics Co. makes the Dormie Neck Support System, a device intended for neck support.
The Dormie Neck Support System is classified as Class I and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Dormie Neck Support System Ref K930730
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Western Diagnostics Co. have in the registry?
The registry currently lists 1 device for The Western Diagnostics Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Western Diagnostics Co.'s devices?
Among its 1 most recently registered device, The Western Diagnostics Co. has devices listed in FDA 510(k) (1 device).
What risk classes do The Western Diagnostics Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for The Western Diagnostics Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from The Western Diagnostics Co. in the registry?
The most recently registered devices listed for The Western Diagnostics Co. include DORMIE NECK SUPPORT SYSTEM.