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FDA Device Info: Letters sent by FDA to manufacturers of Automated External Defibrillators (AEDs)
FDA Device Info: Letters sent by FDA to manufacturers of Automated External Defibrillators (AEDs)
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Request: Letters sent by FDA to manufacturers of Automated External Defibrillators (AEDs) and any necessary accessories, e.g., batteries and defibrillation pads, asking them to provide FDA with an end of life plan for legacy AEDs and accessories that were not submitted in a PMA or not expected to be submitted in a PMA to FDA but were still out in the field.
Request Year: 2019
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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