Tunstall Healthcare
NorwayFDA 510(k) applicant, unverified
- Devices
- 1
What Tunstall Healthcare makes
Tunstall Healthcare manufactures the RTX 3371, which is a Class II medical device.
The company is based in the US and the RTX 3371 is listed in the FDA 510(k) registry.
Catalogue
Rtx 3371 Ref K090886
510(k) 510(k)
Frequently asked questions
How many devices does Tunstall Healthcare have in the registry?
The registry currently lists 1 device for Tunstall Healthcare. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tunstall Healthcare's devices?
Among its 1 most recently registered device, Tunstall Healthcare has devices listed in FDA 510(k) (1 device).
What risk classes do Tunstall Healthcare's devices fall under?
Among its 1 most recently registered device, the classes recorded for Tunstall Healthcare's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tunstall Healthcare in the registry?
The most recently registered devices listed for Tunstall Healthcare include RTX 3371.