Via Biomedical, Inc.
Country not established
- Devices
- 1
What Via Biomedical, Inc. makes
Via Biomedical, Inc. manufactures stent graft balloon catheters, which are used in endovascular procedures to deliver and deploy stent grafts within blood vessels, often for treating aneurysms or vascular occlusions.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Stent Graft Balloon Catheter Ref K091624
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Via Biomedical, Inc. have in the registry?
The registry currently lists 1 device for Via Biomedical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Via Biomedical, Inc.'s devices?
Among its 1 most recently registered device, Via Biomedical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Via Biomedical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Via Biomedical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Via Biomedical, Inc. in the registry?
The most recently registered devices listed for Via Biomedical, Inc. include STENT GRAFT BALLOON CATHETER.