Willowtech
Country not established
- Devices
- 1
What Willowtech makes
Willowtech manufactures endotracheal suction tubes, which are used for airway management and removal of secretions in clinical settings.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Endotracheal Suctiontube Ref K913876
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Willowtech have in the registry?
The registry currently lists 1 device for Willowtech. Devices recorded under merged duplicate company entries are counted once.
Which registries list Willowtech's devices?
Among its 1 most recently registered device, Willowtech has devices listed in FDA 510(k) (1 device).
What risk classes do Willowtech's devices fall under?
Among its 1 most recently registered device, the classes recorded for Willowtech's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Willowtech in the registry?
The most recently registered devices listed for Willowtech include ENDOTRACHEAL SUCTIONTUBE.