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Business · 05/10/2023

FDA Revokes Emergency Use Authorizations for COVID-19 Diagnostic Devices

The US Food and Drug Administration (FDA) has revoked 11 emergency use authorizations for COVID-19 diagnostic devices, including tests from companies such as Luminostics, Inc., NeuMoDx Molecular, Inc., and Exact Sciences Laboratories, due to a request from the authorization holders.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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