Necessary Automated External Defibrillator Accessories: Policy Regarding Compliance Date Guidance for Industry, Stakeholders, Health Care Professionals, and Food and Drug Administration Staff October 2020
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Guidance Issuing OfficeCenter for Devices and Radiological Health
FDA is issuing this guidance to revise its compliance policy regarding the deadline for filing premarket approval (PMA) applications for previously cleared accessories necessary to the operation of automated external defibrillator (AED)1 systems. This policy is based, in part, in consideration of the burden on healthcare facilities as they transition to FDA-approved AEDs and on the manufacturers as they prepare to implement the PMA requirements while addressing the challenges related to Coronavirus Disease 2019 (COVID-19).
This guidance is being implemented without prior public comment because FDA has determined that prior public participation for this guidance is not feasible or appropriate (see section 701(h)(1)(C) of the 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.
1 On February 3, 2015, FDA published a final rule calling for the submission of premarket approval applications for AEDs and their necessary accessories (80 FR 5674). AEDs that were cleared prior to the implementation of this regulatory requirement are sometimes referred to as “legacy” AEDs.
You can submit online or written comments on any guidance at any time (see 21 CFR 10.115(g)(5))
If unable to submit comments online, please mail written comments to:
Food and Drug Administration
5630 Fishers Lane, Rm 1061
Rockville, MD 20852
All written comments should be identified with this document's docket number: FDA-2020-D-1877.