Zdrowie i gospodarka · 05/06/2020

FDA Announces Authorization of Emergency Use of Certain Medical Devices During COVID-19

The US Food and Drug Administration (FDA) has issued and reissued Emergency Use Authorizations (EUAs) for medical devices related to COVID-19, following a public health emergency declaration in February 2020, to facilitate the emergency use of authorized products, including in vitro diagnostics, personal respiratory protective devices, and medical devices.