Vastek
Country not established
- Devices
- 1
What Vastek makes
Vastek manufactures an angioplasty inflator, a device used to deploy and inflate balloons within coronary or peripheral arteries during percutaneous interventions.
The company’s angioplasty inflator is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) premarket notification process. The product is regulated under US jurisdiction.
Catalogue
Angioplasty Inflator Ref K911295
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vastek have in the registry?
The registry currently lists 1 device for Vastek. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vastek's devices?
Among its 1 most recently registered device, Vastek has devices listed in FDA 510(k) (1 device).
What risk classes do Vastek's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vastek's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vastek in the registry?
The most recently registered devices listed for Vastek include ANGIOPLASTY INFLATOR.