Quest Diagnostics has received FDA 510(k) clearance for its Simplexa C difficile Universal Direct Test on the 3M Integrated Cycler.
Subscribe to our email newsletter
The test, which uses a proprietary chemistry that eliminates the need for nucleic-acid extraction, is performed on liquid or unformed human stool samples and detects the toxin B gene (tcdB) of C difficile, including NAP1.
Simplexa tests, running on the 3M Integrated Cycler, employ real-time polymerase chain reaction (RT-PCR) to qualitatively detect viruses, bacteria and other analytes.
Quest Diagnostics and Focus Diagnostics infectious disease medical director Jay Lieberman said: "Fast, reliable PCR tests that are highly specific and sensitive in the detection of the tcdB gene, a toxin-B producing gene of C. difficile, are essential for identifying and treating this infection as well as containing its spread."
Advertise With UsAdvertise on our extensive network of industry websites and newsletters.
Get the PBR newsletterSign up to our free email to get all the latest PBR
news.