Business · 05/10/2023Updated: 10/17/2026 · 1 min read
FDA Revokes Emergency Use Authorizations for COVID-19 Diagnostic Devices
Summary
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 →