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FDA clears TechLab's E. histolytica infection test

The FDA has given TechLab 510(k) clearance for its E. Histolytica Quik Chek test, a rapid membrane enzyme immunoassay that detects Entamoeba histolytica in fecal samples. The test, which has no cross-reactivity with nonpathogenic Entamoeba dispar, produces results in 30 minutes.

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