Medical Instruments Corporation, AG
SwitzerlandFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Modification To: Pronto Dry Ref K002451
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Instruments Corporation, AG have in the registry?
The registry currently lists 1 device for Medical Instruments Corporation, AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Instruments Corporation, AG's devices?
Among its 1 most recently registered device, Medical Instruments Corporation, AG has devices listed in FDA 510(k) (1 device).
What risk classes do Medical Instruments Corporation, AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medical Instruments Corporation, AG's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Medical Instruments Corporation, AG in the registry?
The most recently registered devices listed for Medical Instruments Corporation, AG include MODIFICATION TO: PRONTO DRY.