Licher Medizintechnologie GmbH
GermanyFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Lmt-Kath-S; Lmt-Kath-I Ref K062308
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Licher Medizintechnologie GmbH have in the registry?
The registry currently lists 1 device for Licher Medizintechnologie GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Licher Medizintechnologie GmbH's devices?
Among its 1 most recently registered device, Licher Medizintechnologie GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Licher Medizintechnologie GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Licher Medizintechnologie GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Licher Medizintechnologie GmbH in the registry?
The most recently registered devices listed for Licher Medizintechnologie GmbH include LMT-KATH-S; LMT-KATH-I.