Avant Medical Corporation
Country not established
- Devices
- 1
What Avant Medical Corporation makes
Avant Medical Corporation manufactures the AVANT GUARDIAN 101, a medical device designed for vascular access and monitoring in critical care settings, including central venous catheterization and fluid management applications.
The company’s portfolio is regulated under FDA Class II devices, with the AVANT GUARDIAN 101 authorised via the 510(k) clearance pathway. The device is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Avant Guardian 101 Ref K024018
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Avant Medical Corporation have in the registry?
The registry currently lists 1 device for Avant Medical Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Avant Medical Corporation's devices?
Among its 1 most recently registered device, Avant Medical Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Avant Medical Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Avant Medical Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Avant Medical Corporation in the registry?
The most recently registered devices listed for Avant Medical Corporation include AVANT GUARDIAN 101.