Fiegert-Endotech Medizintechnik GmbH
GermanyFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Fiegert Endotech Flexible Fiberoptic Endoscopes, Fiegert Endotech Flexible Video-Endoscopes Ref K974493
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fiegert-Endotech Medizintechnik GmbH have in the registry?
The registry currently lists 1 device for Fiegert-Endotech Medizintechnik GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fiegert-Endotech Medizintechnik GmbH's devices?
Among its 1 most recently registered device, Fiegert-Endotech Medizintechnik GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Fiegert-Endotech Medizintechnik GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Fiegert-Endotech Medizintechnik GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fiegert-Endotech Medizintechnik GmbH in the registry?
The most recently registered devices listed for Fiegert-Endotech Medizintechnik GmbH include FIEGERT ENDOTECH FLEXIBLE FIBEROPTIC ENDOSCOPES, FIEGERT ENDOTECH FLEXIBLE VIDEO-ENDOSCOPES.