Cci
Country not established
- Devices
- 1
What Cci makes
The company produces the CCI Videokeratoscope/Comparator, a diagnostic device used for assessing corneal topography and refractive error in ophthalmology. This instrument visually compares corneal curvature maps to aid in the evaluation of conditions like astigmatism or post-surgical assessment.
The device falls under FDA Class I regulation and is listed via the 510(k) pathway. It is manufactured in the United States.
Catalogue
Cci Videokeratoscope/Comparator Ref K913022
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cci have in the registry?
The registry currently lists 1 device for Cci. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cci's devices?
Among its 1 most recently registered device, Cci has devices listed in FDA 510(k) (1 device).
What risk classes do Cci's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cci's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Cci in the registry?
The most recently registered devices listed for Cci include CCI VIDEOKERATOSCOPE/COMPARATOR.