Business · 04/12/2020Updated: 10/17/2026 · 1 min read
FDA Revokes Emergency Use Authorizations for Certain Medical Devices
Summary
The Food and Drug Administration (FDA) has revoked the Emergency Use Authorizations for protective barrier enclosures and infusion pumps, citing reasons outlined in the document, following previous revocations in August and September 2020.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →