KALR STORZ SE & Co. KG
GermanyFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
KARL STORZ TIPCAM1 Rubina Ref K262547
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does KALR STORZ SE & Co. KG have in the registry?
The registry currently lists 1 device for KALR STORZ SE & Co. KG. Devices recorded under merged duplicate company entries are counted once.
Which registries list KALR STORZ SE & Co. KG's devices?
Among its 1 most recently registered device, KALR STORZ SE & Co. KG has devices listed in FDA 510(k) (1 device).
What risk classes do KALR STORZ SE & Co. KG's devices fall under?
Among its 1 most recently registered device, the classes recorded for KALR STORZ SE & Co. KG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from KALR STORZ SE & Co. KG in the registry?
The most recently registered devices listed for KALR STORZ SE & Co. KG include KARL STORZ TIPCAM1 Rubina.