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Revvity, Inc. RVTY announced the receipt of the FDAâs 510(k) clearance for EUROIMMUNâs automated chemiluminescence-based immunoassay (ChLIA) test for free testosterone. Per management, it is currently the only FDA-cleared ChLIA assay for direct quantitative measurement of free testosterone in human serum or plasma.
The results on EUROIMMUNâs ChLIA platforms are expected to be rapidly available, with the first result available under an hour (in 48 minutes). It also has an estimate...
>>> Read more: RVTY Stock Falls Despite FDA Nod for Automated Testosterone Test
The results on EUROIMMUNâs ChLIA platforms are expected to be rapidly available, with the first result available under an hour (in 48 minutes). It also has an estimate...
>>> Read more: RVTY Stock Falls Despite FDA Nod for Automated Testosterone Test