Sanovas, Inc.
Country not established
- Devices
- 1
What Sanovas, Inc. makes
Sanovas, Inc. manufactures the PulmoVia Working Channel, a device designed for use in bronchoscopy procedures to facilitate airway access and intervention.
The PulmoVia Working Channel 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
PulmoVia Working Channel Ref K150280
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sanovas, Inc. have in the registry?
The registry currently lists 1 device for Sanovas, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sanovas, Inc.'s devices?
Among its 1 most recently registered device, Sanovas, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sanovas, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sanovas, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sanovas, Inc. in the registry?
The most recently registered devices listed for Sanovas, Inc. include PulmoVia Working Channel.