John W. King
Country not established
- Devices
- 1
What John W. King makes
John W. King manufactures the DISTRAX, a device designed to assist in the management of postoperative pain by delivering continuous peripheral nerve blocks.
The DISTRAX is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Distrax Ref K080542
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does John W. King have in the registry?
The registry currently lists 1 device for John W. King. Devices recorded under merged duplicate company entries are counted once.
Which registries list John W. King's devices?
Among its 1 most recently registered device, John W. King has devices listed in FDA 510(k) (1 device).
What risk classes do John W. King's devices fall under?
Among its 1 most recently registered device, the classes recorded for John W. King's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from John W. King in the registry?
The most recently registered devices listed for John W. King include DISTRAX.