Voronoi Health Analytics Incorporated
CanadaFDA 510(k) applicant, unverified
- Devices
- 1
What Voronoi Health Analytics Incorporated makes
Voronoi Health Analytics Incorporated develops the Data Analysis Facilitation Suite (DAFS), a software tool designed to assist in processing and interpreting clinical or diagnostic data for healthcare providers.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II medical devices and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Data Analysis Facilitation Suite (DAFS) Ref K253944
510(k) 510(k)
Frequently asked questions
How many devices does Voronoi Health Analytics Incorporated have in the registry?
The registry currently lists 1 device for Voronoi Health Analytics Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Voronoi Health Analytics Incorporated's devices?
Among its 1 most recently registered device, Voronoi Health Analytics Incorporated has devices listed in FDA 510(k) (1 device).
What risk classes do Voronoi Health Analytics Incorporated's devices fall under?
Among its 1 most recently registered device, the classes recorded for Voronoi Health Analytics Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Voronoi Health Analytics Incorporated in the registry?
The most recently registered devices listed for Voronoi Health Analytics Incorporated include Data Analysis Facilitation Suite (DAFS).