BC Week In Review | May 12, 2014
Clinical News

Artus C regulatory update

FDA granted 510(k) clearance to the QIAsymphony RGQ MDx system and the artus C. difficile QS-RGQ MDx Kit to quantitatively detect Clostridium difficile. The kit has CE Mark approval in Europe for use on the...
BC Week In Review | Feb 10, 2014
Clinical News

Artus C regulatory update

Intelligent Medical Devices said the artus C. difficile QS-RGQ Kit received CE Mark approval for use with Qiagen's QIAsymphony SP/AS and Rotor-Gene Q instruments to aid in diagnosing Clostridium difficile infection. The kit detects toxigenic...
Items per page:
1 - 2 of 2