Invasatec
Country not established
- Devices
- 2
What Invasatec makes
Invasatec manufactures an angiographic contrast management system consisting of a Part A and Part B, as well as the Acist angiographic injector, both of which are devices used to deliver contrast media during imaging procedures.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. Invasatec is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Acist Angiographic Injector Ref K963982
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Invasatec have in the registry?
The registry currently lists 2 devices for Invasatec. Devices recorded under merged duplicate company entries are counted once.
Which registries list Invasatec's devices?
Among its 2 most recently registered devices, Invasatec has devices listed in FDA 510(k) (2 devices).
What risk classes do Invasatec's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Invasatec's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Invasatec in the registry?
The most recently registered devices listed for Invasatec include ANGIOGRAPHIC CONTRAST MANAGEMENT SYSTEM, MODEL PART A AND PART B and ACIST ANGIOGRAPHIC INJECTOR.