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Cystic Fibrosis

LUMINEX RECEIVES 510(k) CLEARANCE FOR NEW CYSTIC FIBROSIS TEST

Published in Healthcare Mergers, Acquisitions and Ventures Week, September 26th, 2009

Luminex Corporation (NASDAQ: LMNX), the worldwide leader in multiplexed solutions, 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.

Designed with years of feedback from clinicians and technicians, the newly cleared xTAG test detects for 39 CF-causing gene mutations. It is used to screen potential parents to determine if they are carriers of CF-causing gene mutations, and as an aid in newborn screening and in confirmatory diagnostic testing in newborns and children.

Cystic fibrosis is a chronic inherited genetic disease...

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