Arbor Vita Corportation
Country not established
- Devices
- 1
What Arbor Vita Corportation makes
Arbor Vita Corporation manufactures the AVC A/H5N1 Flu Test, a diagnostic device designed for detecting the H5N1 avian influenza virus in clinical samples.
This product is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Avc A/H5N1 Flu Test Ref K083278
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arbor Vita Corportation have in the registry?
The registry currently lists 1 device for Arbor Vita Corportation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arbor Vita Corportation's devices?
Among its 1 most recently registered device, Arbor Vita Corportation has devices listed in FDA 510(k) (1 device).
What risk classes do Arbor Vita Corportation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Arbor Vita Corportation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arbor Vita Corportation in the registry?
The most recently registered devices listed for Arbor Vita Corportation include AVC A/H5N1 FLU TEST.