10/08/2020 12:00 AM EDT
Source: U.S. Food and Drug Administration (FDA). Published: 10/8/2020. This three-page fact sheet informs healthcare providers of the significant known and potential risks and benefits of the emergency use of the Access SARS‐CoV‐2 IgM. The Access SARS‐CoV‐2 IgM is authorized for the detection of antibodies to SARS-CoV-2 in human serum and plasma. (PDF)
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