Pulsonic AG, Medical Technology
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Cardioscope Sonoplus 3000 Ref K051126
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pulsonic Ag, Medical Technology have in the registry?
The registry currently lists 1 device for Pulsonic Ag, Medical Technology. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pulsonic Ag, Medical Technology's devices?
Among its 1 most recently registered device, Pulsonic Ag, Medical Technology has devices listed in FDA 510(k) (1 device).
What risk classes do Pulsonic Ag, Medical Technology's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pulsonic Ag, Medical Technology's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pulsonic Ag, Medical Technology in the registry?
The most recently registered devices listed for Pulsonic Ag, Medical Technology include CARDIOSCOPE SONOPLUS 3000.