Philips Medical Systems Netherland BV
NetherlandsFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Philips Medical Systems Netherland BV have in the registry?
The registry currently lists 1 device for Philips Medical Systems Netherland BV. Devices recorded under merged duplicate company entries are counted once.
Which registries list Philips Medical Systems Netherland BV's devices?
Among its 1 most recently registered device, Philips Medical Systems Netherland BV has devices listed in FDA 510(k) (1 device).
What risk classes do Philips Medical Systems Netherland BV's devices fall under?
Among its 1 most recently registered device, the classes recorded for Philips Medical Systems Netherland BV's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Philips Medical Systems Netherland BV in the registry?
The most recently registered devices listed for Philips Medical Systems Netherland BV include ALLURA XPER FD SERIES / ALLURA XPER OR TABLE SERIES.