Kist Intl.
Country not established
- Devices
- 1
What Kist Intl. makes
Kist Intl. manufactures the HyperFree, a device designed for cryogenic or rapid-freezing applications in medical or laboratory settings.
The HyperFree is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Hyperfree Ref K913527
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kist Intl. have in the registry?
The registry currently lists 1 device for Kist Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kist Intl.'s devices?
Among its 1 most recently registered device, Kist Intl. has devices listed in FDA 510(k) (1 device).
What risk classes do Kist Intl.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kist Intl.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Kist Intl. in the registry?
The most recently registered devices listed for Kist Intl. include HYPERFREE.