MALVERN, Penn.--(BUSINESS WIRE)--Fujirebio Diagnostics, Inc. (FDI) received approval from the Food & Drug Administration (FDA) under the Humanitarian Device Exemption (HDE) program for the MESOMARK® Assay, the world’s first in-vitro test for mesothelioma, a form of cancer linked to asbestos exposure. Via a simple blood test, the MESOMARK test enables doctors to monitor patients diagnosed with biphasic or epithelioid mesothelioma.
