07:00 , May 12, 2014 |  BC Week In Review  |  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...
08:00 , Feb 10, 2014 |  BC Week In Review  |  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...