Asset Medikal
TürkiyeFDA applicant, unverified
- Devices
- 1
What Asset Medikal makes
Asset Medikal produces the FlowArt® Vial Access Device Vented, a vented system designed for secure and sterile access to vial contents in medical settings.
This device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
FlowArt® Vial Access Device Vented Ref K251715
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Asset Medikal have in the registry?
The registry currently lists 1 device for Asset Medikal. Devices recorded under merged duplicate company entries are counted once.
Which registries list Asset Medikal's devices?
Among its 1 most recently registered device, Asset Medikal has devices listed in FDA 510(k) (1 device).
What risk classes do Asset Medikal's devices fall under?
Among its 1 most recently registered device, the classes recorded for Asset Medikal's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Asset Medikal in the registry?
The most recently registered devices listed for Asset Medikal include FlowArt® Vial Access Device Vented.