Cryofos Medical GmbH
GermanyFDA 510(k) applicant, unverified
- Devices
- 1
What Cryofos Medical GmbH makes
Cryofos Medical GmbH makes the Cryofos device, which is a cryotherapy system used for medical applications.
The Cryofos device is classified as Class II and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Cryofos Ref K170810
510(k) 510(k)
Frequently asked questions
How many devices does Cryofos Medical GmbH have in the registry?
The registry currently lists 1 device for Cryofos Medical GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cryofos Medical GmbH's devices?
Among its 1 most recently registered device, Cryofos Medical GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Cryofos Medical GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cryofos Medical GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cryofos Medical GmbH in the registry?
The most recently registered devices listed for Cryofos Medical GmbH include CRYOFOS.