Barcoview Mis Edinburgh
United KingdomFDA applicant, unverified
- Devices
- 3
What Barcoview Mis Edinburgh makes
Barcoview Mis Edinburgh manufactures the VOXAR 3D Enterprise imaging system, including versions integrated with Cardiametrix and Colonmetrix, as well as a variant combined with PET/CT perfusion. These products are designed for advanced 3D medical imaging and diagnostic analysis.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. The devices are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Voxar 3D Enterprise, Model 6.1 Ref K060505
Regimes: 510(k) Registry: 510(k)Voxar 3D Enterprise With Cardiametrix Ref K061326
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Barcoview Mis Edinburgh have in the registry?
The registry currently lists 3 devices for Barcoview Mis Edinburgh. Devices recorded under merged duplicate company entries are counted once.
Which registries list Barcoview Mis Edinburgh's devices?
Among its 3 most recently registered devices, Barcoview Mis Edinburgh has devices listed in FDA 510(k) (3 devices).
What risk classes do Barcoview Mis Edinburgh's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Barcoview Mis Edinburgh's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Barcoview Mis Edinburgh in the registry?
The most recently registered devices listed for Barcoview Mis Edinburgh include VOXAR 3D ENTERPRISE, MODEL 6.1, VOXAR 3D ENTERPRISE WITH CARDIAMETRIX and VOXAR 3D ENTERPRISE WITH COLONMETRIX AND PET/CT PERFUSION.