Caditec AG
Country not established
- Devices
- 1
What Caditec AG makes
Caditec AG manufactures the CADISCOPE electronic stethoscope, a medical device used for auscultation.
The company is based in the US and its products are listed in the FDA 510(k) registry as Class II medical devices.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Cadiscope Electronic Stethoscope Ref K990809
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Caditec AG have in the registry?
The registry currently lists 1 device for Caditec AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Caditec AG's devices?
Among its 1 most recently registered device, Caditec AG has devices listed in FDA 510(k) (1 device).
What risk classes do Caditec AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Caditec AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Caditec AG in the registry?
The most recently registered devices listed for Caditec AG include CADISCOPE ELECTRONIC STETHOSCOPE.