Monica Veytia
Country not established
- Devices
- 1
What Monica Veytia makes
Monica Veytia manufactures the Kanteron DICOM Station (KDS), Model 3.0, a software-based system designed for medical image management and viewing, adhering to DICOM standards for interoperability in healthcare settings.
The Kanteron DICOM Station (KDS), Model 3.0 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The manufacturer operates from the United States.
Catalogue
Kanteron Dicom Station (Kds), Model 3.0 Ref K073176
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Monica Veytia have in the registry?
The registry currently lists 1 device for Monica Veytia. Devices recorded under merged duplicate company entries are counted once.
Which registries list Monica Veytia's devices?
Among its 1 most recently registered device, Monica Veytia has devices listed in FDA 510(k) (1 device).
What risk classes do Monica Veytia's devices fall under?
Among its 1 most recently registered device, the classes recorded for Monica Veytia's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Monica Veytia in the registry?
The most recently registered devices listed for Monica Veytia include KANTERON DICOM STATION (KDS), MODEL 3.0.