Cynovad
CanadaFDA 510(k) applicant, unverified
- Devices
- 1
What Cynovad makes
Cynovad manufactures the CYNOVAD ZIRKON, which is a Class II medical device.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
Cynovad Zirkon Ref K023327
510(k) 510(k)
Frequently asked questions
How many devices does Cynovad have in the registry?
The registry currently lists 1 device for Cynovad. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cynovad's devices?
Among its 1 most recently registered device, Cynovad has devices listed in FDA 510(k) (1 device).
What risk classes do Cynovad's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cynovad's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cynovad in the registry?
The most recently registered devices listed for Cynovad include CYNOVAD ZIRKON.