Eureka AB
SwedenFDA 510(k) applicant, unverified
- Devices
- 1
What Eureka AB makes
Eureka AB manufactures the VARITEST, a medical device designed for testing and validation of variable parameters in clinical or laboratory settings.
The VARITEST is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Varitest Ref K882547
510(k) 510(k)
Frequently asked questions
How many devices does Eureka AB have in the registry?
The registry currently lists 1 device for Eureka AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eureka AB's devices?
Among its 1 most recently registered device, Eureka AB has devices listed in FDA 510(k) (1 device).
What risk classes do Eureka AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Eureka AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eureka AB in the registry?
The most recently registered devices listed for Eureka AB include VARITEST.