Richter & Rothe AG
GermanyFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Kavs - Catheter, Models 1107100 & 1107060 Ref K052844
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Richter & Rothe AG have in the registry?
The registry currently lists 1 device for Richter & Rothe AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Richter & Rothe AG's devices?
Among its 1 most recently registered device, Richter & Rothe AG has devices listed in FDA 510(k) (1 device).
What risk classes do Richter & Rothe AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Richter & Rothe AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Richter & Rothe AG in the registry?
The most recently registered devices listed for Richter & Rothe AG include KAVS - CATHETER, MODELS 1107100 & 1107060.