FDA approves new xTAG Cystic Fibrosis 39 Kit v2 from Luminex
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FDA approves new xTAG Cystic Fibrosis 39 Kit v2 from Luminex
Luminex Corporation (NASDAQ: LMNX), the worldwide leader in multiplexed solutions, today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for a new cystic fibrosis (CF) test: the xTAG® Cystic Fibrosis 39 Kit v2.
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Tags: Genetic, Cystic Fibrosis, Drug, FDA
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