Csist
Country not established
- Devices
- 1
What Csist makes
Csist develops a DICOM Gateway/Image Manager for medical imaging data integration, enabling secure transfer and storage of diagnostic images and related information within healthcare networks.
The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) clearance pathway. Csist is headquartered in the United States.
Catalogue
Csist Dicom Gateway/Image Manager Ref K012327
510(k) 510(k)
Frequently asked questions
How many devices does Csist have in the registry?
The registry currently lists 1 device for Csist. Devices recorded under merged duplicate company entries are counted once.
Which registries list Csist's devices?
Among its 1 most recently registered device, Csist has devices listed in FDA 510(k) (1 device).
What risk classes do Csist's devices fall under?
Among its 1 most recently registered device, the classes recorded for Csist's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Csist in the registry?
The most recently registered devices listed for Csist include CSIST DICOM GATEWAY/IMAGE MANAGER.