Artivent Corporation
Country not established
- Devices
- 1
What Artivent Corporation makes
Artivent Corporation manufactures the SAVE Resuscitator, a manual resuscitation device designed for emergency use in neonatal and pediatric patients to provide positive-pressure ventilation during resuscitation.
The SAVE Resuscitator 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
Save Resuscitator Ref K073410
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Artivent Corporation have in the registry?
The registry currently lists 1 device for Artivent Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Artivent Corporation's devices?
Among its 1 most recently registered device, Artivent Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Artivent Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Artivent Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Artivent Corporation in the registry?
The most recently registered devices listed for Artivent Corporation include SAVE RESUSCITATOR.