Varioraw SA
Country not established
- Devices
- 1
What Varioraw SA makes
Varioraw SA manufactures the FLUTTER®, a medical device designed for monitoring and analyzing cardiac flutter activity in patients, likely used for diagnostic or research purposes in electrophysiology studies.
The FLUTTER® is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Flutter(R) Ref K940986
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Varioraw SA have in the registry?
The registry currently lists 1 device for Varioraw SA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Varioraw SA's devices?
Among its 1 most recently registered device, Varioraw SA has devices listed in FDA 510(k) (1 device).
What risk classes do Varioraw SA's devices fall under?
Among its 1 most recently registered device, the classes recorded for Varioraw SA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Varioraw SA in the registry?
The most recently registered devices listed for Varioraw SA include FLUTTER(R).