Iverness Medical Professional Diagnostics
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Modification To Biostar Oia Shigatox Ref K071799
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Iverness Medical Professional Diagnostics have in the registry?
The registry currently lists 1 device for Iverness Medical Professional Diagnostics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Iverness Medical Professional Diagnostics's devices?
Among its 1 most recently registered device, Iverness Medical Professional Diagnostics has devices listed in FDA 510(k) (1 device).
What risk classes do Iverness Medical Professional Diagnostics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Iverness Medical Professional Diagnostics's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Iverness Medical Professional Diagnostics in the registry?
The most recently registered devices listed for Iverness Medical Professional Diagnostics include MODIFICATION TO BIOSTAR OIA SHIGATOX.