Home » FDI Submits Application to FDA for Approval of MESOMARK
FDI Submits Application to FDA for Approval of MESOMARK
May 4, 2005
Fujirebio Diagnostics (FDI), a company specializing in oncology testing, announced that it submitted a 510(k) application to the FDA for clearance of MESOMARK, the first blood test for mesothelioma.
Genetic Engineering News (http://www.genengnews.com/news/bnitem.aspx?name=517506XSL_NEWSML_TO_NEWSML_WEB.xml)
(http://www.genengnews.com/news/bnitem.aspx?name=517506XSL_NEWSML_TO_NEWSML_WEB.xml)
KEYWORDS FDAnews Device Daily Bulletin
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