West Lake Marketing
Country not established
- Devices
- 1
What West Lake Marketing makes
West Lake Marketing makes the PALS device.
The PALS device is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pals Ref K863621
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does West Lake Marketing have in the registry?
The registry currently lists 1 device for West Lake Marketing. Devices recorded under merged duplicate company entries are counted once.
Which registries list West Lake Marketing's devices?
Among its 1 most recently registered device, West Lake Marketing has devices listed in FDA 510(k) (1 device).
What risk classes do West Lake Marketing's devices fall under?
Among its 1 most recently registered device, the classes recorded for West Lake Marketing's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from West Lake Marketing in the registry?
The most recently registered devices listed for West Lake Marketing include PALS.