Aetmed, S.p.A.
Country not established
- Devices
- 1
What Aetmed, S.p.A. makes
Aetmed, S.P.A. makes image processing software for medical use.
The company's devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Aetmed Image Processing Software Ref K012093
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aetmed, S.P.A. have in the registry?
The registry currently lists 1 device for Aetmed, S.P.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aetmed, S.P.A.'s devices?
Among its 1 most recently registered device, Aetmed, S.P.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Aetmed, S.P.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aetmed, S.P.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aetmed, S.P.A. in the registry?
The most recently registered devices listed for Aetmed, S.P.A. include AETMED IMAGE PROCESSING SOFTWARE.