Philips Volcano
Country not established
- Devices
- 2
What Philips Volcano makes
Philips Volcano makes the FFR V2.5 and Pioneer Plus Catheter devices.
These devices are Class II medical devices listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ffr V2.5 Ref K170133
Regimes: 510(k) Registry: 510(k)Pioneer Plus Catheter Ref K162418
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Philips Volcano have in the registry?
The registry currently lists 2 devices for Philips Volcano. Devices recorded under merged duplicate company entries are counted once.
Which registries list Philips Volcano's devices?
Among its 2 most recently registered devices, Philips Volcano has devices listed in FDA 510(k) (2 devices).
What risk classes do Philips Volcano's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Philips Volcano's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Philips Volcano in the registry?
The most recently registered devices listed for Philips Volcano include FFR V2.5 and Pioneer Plus Catheter.