Philips Image Guided Therapy Devices
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- Devices
- 1
What Philips Image Guided Therapy Devices makes
Philips Image Guided Therapy Devices manufactures the Bridge Plus Occlusion Balloon, a Class II medical device designed for vascular occlusion procedures.
The Bridge Plus Occlusion Balloon is regulated under the FDA’s 510(k) pathway and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Bridge Plus Occlusion Balloon (590-002) Ref K251358
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Philips Image Guided Therapy Devices have in the registry?
The registry currently lists 1 device for Philips Image Guided Therapy Devices. Devices recorded under merged duplicate company entries are counted once.
Which registries list Philips Image Guided Therapy Devices's devices?
Among its 1 most recently registered device, Philips Image Guided Therapy Devices has devices listed in FDA 510(k) (1 device).
What risk classes do Philips Image Guided Therapy Devices's devices fall under?
Among its 1 most recently registered device, the classes recorded for Philips Image Guided Therapy Devices's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Philips Image Guided Therapy Devices in the registry?
The most recently registered devices listed for Philips Image Guided Therapy Devices include Bridge Plus Occlusion Balloon (590-002).