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Monday, 10/31/2011 12:47:52 PM

Monday, October 31, 2011 12:47:52 PM

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Roche Hldg receives FDA approval for Acute Hepatitis B Test (RHHBY) 41.84 -0.33 : Co announced that the FDA granted Premarket Approval (PMA) for its IgM antibody to hepatitis B core antigen assay for use on the cobas e 601 analyzer, the immunoassay module of the cobas? 6000 analyzer series for mid-volume laboratories. The test represents the final component of the acute panel within the hepatitis test menu for the cobas 6000 series.
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