Vitex
Country not established
- Devices
- 1
What Vitex makes
Vitex makes pre-calibrated pipettes.
These devices are Class I medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Pre-Calibrated Pipettes Ref K834100
510(k) 510(k)
Frequently asked questions
How many devices does Vitex have in the registry?
The registry currently lists 1 device for Vitex. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vitex's devices?
Among its 1 most recently registered device, Vitex has devices listed in FDA 510(k) (1 device).
What risk classes do Vitex's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vitex's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Vitex in the registry?
The most recently registered devices listed for Vitex include PRE-CALIBRATED PIPETTES.