Ekeroth Quality AB
SwedenFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dynawell Or Dynawell Ref K992120
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ekeroth Quality AB have in the registry?
The registry currently lists 1 device for Ekeroth Quality AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ekeroth Quality AB's devices?
Among its 1 most recently registered device, Ekeroth Quality AB has devices listed in FDA 510(k) (1 device).
What risk classes do Ekeroth Quality AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ekeroth Quality AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ekeroth Quality AB in the registry?
The most recently registered devices listed for Ekeroth Quality AB include DYNAWELL OR DYNAWELL.