Slk Medical GmbH
GermanyFDA applicant, unverified
- Devices
- 2
What Slk Medical GmbH makes
Slk Medical GmbH manufactures lymphatic drainage devices, including the VariLymph 12 pro and V12 PRO, which are designed for manual lymphatic drainage therapy.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
VariLymph 12 pro Ref K193476
Regimes: 510(k) Registry: 510(k)V12 Pro Ref K210913
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Slk Medical GmbH have in the registry?
The registry currently lists 2 devices for Slk Medical GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Slk Medical GmbH's devices?
Among its 2 most recently registered devices, Slk Medical GmbH has devices listed in FDA 510(k) (2 devices).
What risk classes do Slk Medical GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Slk Medical GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Slk Medical GmbH in the registry?
The most recently registered devices listed for Slk Medical GmbH include VariLymph 12 pro and V12 PRO.