The FDA Finalizes Transition Plan for Medical Device Authori

The Food and Drug Administration (FDA) has announced transition plans for Emergency Use Authorization (EUA)-authorized medical devices and devices marketed pursuant to COVID-19-related...

Related Keywords

, Public Health Emergency , Drug Administration , Coagulation Systems For Measurement Of Viscoelastic Properties , Foley Hoag , Clinical Laboratory Improvement Amendments , Public Health Service Act , Human Services , Emergency Use Authorization , Transition Plan , Authorized Devices , Related Device Policies , Federal Food , Cosmetic Act , Coronavirus Disease , Policy Transition Plan , Federal Register , Plan Guidance , Transition Implementation Plan , Quality System Regulations , Enforcement Discretion Transition Plan Guidance , Remote Digital Pathology Devices During , Imaging Systems During , Non Invasive Fetal , Maternal Monitoring Devices Used , Support Patient Monitoring During , Telethermographic Systems During , Digital Health Devices , Treating Psychiatric Disorders During , Extracorporeal Membrane Oxygenation , Cardiopulmonary Bypass Devices During , Remote Ophthalmic Assessment , Monitoring Devices During , Infusion Pumps , Accessories During , Face Shields , Surgical Masks , Respirators During , Gloves During , Disinfectant Devices , Air Purifiers During , Molecular Influenza , Viscoelastic Properties , Enforcement Policy During , Health Emergency , Viral Transport Media During ,