FDA issues enforcement policy for ventilators and accessories and other respiratory devices during COVID-19
The Food and Drug Administration (FDA) is issuing guidance to provide a policy to help expand the availability of ventilators as well as other respiratory devices and their accessories during the COVID-19 pandemic.
Read more at HPN.
This policy is intended to remain in effect only for the duration of the public health emergency related to COVID-19 declared by the Department of Health and Human Services (HHS), including any renewals made by the Secretary in accordance with section 319(a)(2) of the PHS Act.
Given this public health emergency, this guidance is being implemented without prior public comment because the FDA has determined that prior public participation for this guidance is not feasible or appropriate (see section 701(h)(1)(C)(i) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) and 21 CFR 10.115(g)(2)). This guidance document is being implemented immediately, but it remains subject to comment in accordance with the Agency's good guidance practices.
