Cryo Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
Catalogue
Cellsoft(Tm)-Casa (Series 1000, 2000 & 3000) Ref K872145
510(k) 510(k)Pulsair I & Ii Ref K833994
510(k) 510(k)Ventilatory Frequency Monitor Ref K834569
510(k) 510(k)
Frequently asked questions
How many devices does Cryo Corp. have in the registry?
The registry currently lists 3 devices for Cryo Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cryo Corp.'s devices?
Among its 3 most recently registered devices, Cryo Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Cryo Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Cryo Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cryo Corp. in the registry?
The most recently registered devices listed for Cryo Corp. include CELLSOFT(TM)-CASA (SERIES 1000, 2000 & 3000), PULSAIR I & II and VENTILATORY FREQUENCY MONITOR.