Western Clinical Technology Systems, Inc.
Country not established
- Devices
- 1
What Western Clinical Technology Systems, Inc. makes
Western Clinical Technology Systems, Inc. makes the Echopulse Muscle Stimulator System, Model 800, a device designed for muscle stimulation therapy.
This device is classified as Class II and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Echopulse Muscle Stimulator System, Model 800 Ref K023230
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Western Clinical Technology Systems, Inc. have in the registry?
The registry currently lists 1 device for Western Clinical Technology Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Western Clinical Technology Systems, Inc.'s devices?
Among its 1 most recently registered device, Western Clinical Technology Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Western Clinical Technology Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Western Clinical Technology Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Western Clinical Technology Systems, Inc. in the registry?
The most recently registered devices listed for Western Clinical Technology Systems, Inc. include ECHOPULSE MUSCLE STIMULATOR SYSTEM, MODEL 800.