by Glenn S. Demby | Mar 23, 2020 | Articles , Clinical Diagnostics Insider , Diagnostic Testing and Emerging Technologies , FDA-dtet , Recent Headlines
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by Glenn S. Demby | Mar 18, 2020 | Articles , CLIA-nir , Essential , Laboratory Industry Report , National Lab Reporter , News-nir
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by Glenn S. Demby | Mar 6, 2020 | Essential , FDA-lir , Industry Buzz-lir , Laboratory Industry Report
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by Glenn S. Demby | Feb 8, 2020 | Essential , FDA-lir , Industry Buzz-lir , Laboratory Industry Report
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by Glenn S. Demby | Jan 24, 2020 | Clinical Diagnostics Insider , Diagnostic Testing and Emerging Technologies , FDA-dtet
On Dec. 30, 2019, the U.S. Food and Drug Administration (FDA) published a final order exempting dozens of Class I and Class II medical devices that previously required 510(k) submission from 510(k) premarket review
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