Keosys SAS
FranceFDA applicant, unverified
- Devices
- 3
What Keosys SAS makes
Keosys Sas manufactures medical imaging devices and software, including the VISIO+CD VIEWER for digital radiograph viewing, the IMAGYS system for advanced medical imaging, and the Advanced Medical Imaging Software Suite (KSWVWR) for diagnostic analysis.
These products are classified as Class II devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Visio+cd Viewer# KPSCDVE01 Ref K070606
Regimes: 510(k) Registry: 510(k)Imagys Ref K102000
Regimes: 510(k) Registry: 510(k)Advanced Medical Imaging Software Suite (KSWVWR) Ref K160334
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Keosys Sas have in the registry?
The registry currently lists 3 devices for Keosys Sas. Devices recorded under merged duplicate company entries are counted once.
Which registries list Keosys Sas's devices?
Among its 3 most recently registered devices, Keosys Sas has devices listed in FDA 510(k) (3 devices).
What risk classes do Keosys Sas's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Keosys Sas's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Keosys Sas in the registry?
The most recently registered devices listed for Keosys Sas include VISIO+CD VIEWER# KPSCDVE01, IMAGYS and Advanced Medical Imaging Software Suite (KSWVWR).