Demonbinder Electronics
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Hyperstethoscope, Model Z 00 Ref K801165
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Demonbinder Electronics have in the registry?
The registry currently lists 1 device for Demonbinder Electronics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Demonbinder Electronics's devices?
Among its 1 most recently registered device, Demonbinder Electronics has devices listed in FDA 510(k) (1 device).
What risk classes do Demonbinder Electronics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Demonbinder Electronics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Demonbinder Electronics in the registry?
The most recently registered devices listed for Demonbinder Electronics include HYPERSTETHOSCOPE, MODEL Z 00.