After February 3, 2021, manufacturers and distributors can no longer support AEDs that do not have FDA premarket approval. Customers will no longer be able to receive service or order accessories (including batteries, cables, and electrodes), so they will need to replace these devices to ensure they are ready for an emergency.
Zoll's PMA info flyer summarizes this mandate to help you and your customers better understand what it means for them. The flyer also provides an up-to-date list of approved devices so your customers will know if their AED has FDA premarket approval.