Ktk Medical Supplies GmbH
GermanyFDA applicant, unverified
- Devices
- 1
What Ktk Medical Supplies GmbH makes
Ktk Medical Supplies GmbH manufactures the BRIGHTGLASS BRIGHTGLASS M device.
The device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
Brightglass Brightglass M Ref K122025
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ktk Medical Supplies GmbH have in the registry?
The registry currently lists 1 device for Ktk Medical Supplies GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ktk Medical Supplies GmbH's devices?
Among its 1 most recently registered device, Ktk Medical Supplies GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Ktk Medical Supplies GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ktk Medical Supplies GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ktk Medical Supplies GmbH in the registry?
The most recently registered devices listed for Ktk Medical Supplies GmbH include BRIGHTGLASS BRIGHTGLASS M.