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Zdrowie i gospodarka · 25/04/2023

FDA Authorizes Emergency Use of Medical Device for COVID-19 Treatment

The US Food and Drug Administration (FDA) has issued an Emergency Use Authorization (EUA) for a medical device related to COVID-19 treatment, following a public health emergency declaration by the Secretary of Health and Human Services in February 2020.

Source: Federal Register — Food and Drug AdministrationOpen original release →