02/29/2020 12:00 AM EST
Source: U.S. Food and Drug Administration (FDA). Published: 2/29/2020. This three-page fact sheet informs healthcare providers of the significant known and potential risks and benefits of the emergency use of the New York SARS-CoV-2 Real-time RT-PCR Diagnostic Panel. The New York SARS-CoV-2 Real-time RT-PCR Diagnostic Panel is authorized for use on respiratory specimens from individuals who meet the Centers for Disease Control and Prevention (CDC) coronavirus disease 2019 (COVID-19) clinical and/or epidemiological criteria. (PDF)
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