Neodynamics AB
SwedenFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
NeoNavia Biopsy System Ref K220595
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neodynamics AB have in the registry?
The registry currently lists 1 device for Neodynamics AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neodynamics AB's devices?
Among its 1 most recently registered device, Neodynamics AB has devices listed in FDA 510(k) (1 device).
What risk classes do Neodynamics AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Neodynamics AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neodynamics AB in the registry?
The most recently registered devices listed for Neodynamics AB include NeoNavia Biopsy System.