Corvascular Diagnostics, LLC
Country not established
- Devices
- 1
What Corvascular Diagnostics, LLC makes
Corvascular Diagnostics, LLC manufactures the VasoGuard family of intravascular imaging catheters, designed for coronary and peripheral vascular assessments. These devices provide real-time cross-sectional imaging to evaluate plaque composition, vessel lumen dimensions, and arterial wall integrity during diagnostic and interventional procedures.
The VasoGuard portfolio is classified under FDA’s Class II regulatory category and is authorised through the 510(k) clearance process. The company is based in the United States, with its devices listed in the FDA’s 510(k) registry.
Catalogue
VasoGuard (V10, V8, V6, V4, V2) Ref K233976
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Corvascular Diagnostics, LLC have in the registry?
The registry currently lists 1 device for Corvascular Diagnostics, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Corvascular Diagnostics, LLC's devices?
Among its 1 most recently registered device, Corvascular Diagnostics, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Corvascular Diagnostics, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Corvascular Diagnostics, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Corvascular Diagnostics, LLC in the registry?
The most recently registered devices listed for Corvascular Diagnostics, LLC include VasoGuard (V10, V8, V6, V4, V2).