Cryosan, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 6
What Cryosan, Inc. makes
Cryosan, Inc. manufactures automated blood cell separators for therapeutic apheresis procedures, circulating cyto-therms for controlled cell culture environments, and infusion pumps for precise fluid administration. The company also produces CRYOSAN Normal Saline, a sterile irrigation solution, and rocking/circulating cyto-therms designed for laboratory applications.
The company’s portfolio includes devices classified as Class I, Class II, and Unclassified (U), with several products authorised via the FDA’s 510(k) pathway. These devices are listed under U.S. regulatory records, and the company operates from the United States.
Catalogue
Automated Blood Cell Separator Ref K822521
510(k) 510(k)Circulating Cyto-Therms Ref K812311
510(k) 510(k)Automated Blood Cell Separator Ref K830831
510(k) 510(k)Cryosan Normal Saline Ref K812309
510(k) 510(k)Infusion Pump Ref K831953
510(k) 510(k)Rocking/Circulating Cyto-Therm Ii 3570 Ref K813489
510(k) 510(k)
Frequently asked questions
How many devices does Cryosan, Inc. have in the registry?
The registry currently lists 6 devices for Cryosan, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cryosan, Inc.'s devices?
Among its 6 most recently registered devices, Cryosan, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Cryosan, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Cryosan, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cryosan, Inc. in the registry?
The most recently registered devices listed for Cryosan, Inc. include AUTOMATED BLOOD CELL SEPARATOR, CIRCULATING CYTO-THERMS, CRYOSAN NORMAL SALINE and INFUSION PUMP.