Willson
Country not established
- Devices
- 2
What Willson makes
Willson manufactures an external jugular CVP catheterization kit, which is a medical device used for central venous pressure monitoring.
The company is based in the US and its products are listed in the FDA 510(k) registry as Class II devices.
Catalogue
Introducer, Percutaneous Ref K812143
Regimes: 510(k) Registry: 510(k)External Jugular Cvp Catherization Kit Ref K802576
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Willson have in the registry?
The registry currently lists 2 devices for Willson. Devices recorded under merged duplicate company entries are counted once.
Which registries list Willson's devices?
Among its 2 most recently registered devices, Willson has devices listed in FDA 510(k) (2 devices).
What risk classes do Willson's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Willson's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Willson in the registry?
The most recently registered devices listed for Willson include INTRODUCER, PERCUTANEOUS and EXTERNAL JUGULAR CVP CATHERIZATION KIT.