We use cookies on our websites to ensure the proper functioning of the website and to help provide the best user experience.
By continuing to use our site, you agree to the use of cookies. Learn more about cookies here.


QuikRead go® CRP test cleared in the US

Orion Diagnostica’s QuikRead go CRP test received clearance from the US FDA to market the device for clinical laboratories in the US. The QuikRead go test system measures C-reactive protein in whole blood, plasma and serum in only 2 minutes. The test system consists of a small device and a ready-to-use CRP reagent kit with all the required materials for performing the test. This easy-to-use system is in wide use worldwide.

QuikRead go CRP FDA clearance in the FDA 510(k) premarket notification database


More product information for the US product version will follow. 

Read about Orion Diagnostica