Cryo2 Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Cryo2 Corp. makes
Cryo2 Corp. manufactures the MAXAMAN device and a Cardiac Event Recorder, both of which are medical devices intended for cardiac monitoring and related applications.
These products are classified as Class II medical devices and are listed in the FDA 510(k) registry. Cryo2 Corp. is based in the United States.
Catalogue
Maxaman Ref K841893
510(k) 510(k)Cardiac Event Recorder Ref K843533
510(k) 510(k)
Frequently asked questions
How many devices does Cryo2 Corp. have in the registry?
The registry currently lists 2 devices for Cryo2 Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cryo2 Corp.'s devices?
Among its 2 most recently registered devices, Cryo2 Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cryo2 Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cryo2 Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cryo2 Corp. in the registry?
The most recently registered devices listed for Cryo2 Corp. include MAXAMAN and CARDIAC EVENT RECORDER.