PMA supplement
P160015 S020: AED Plus, AED 3, X Series, R Series, Propaq MD, AED Pro, AED 3 BLS
FDA PMA supplement · Normal 180 Day Track No User Fee · ZOLL Medical Corporation
Key facts
| Original PMA | P160015 |
|---|---|
| Supplement number | S020 |
| Supplement type | Normal 180 Day Track No User Fee |
| Reason for the supplement | Location Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | AED Plus, AED 3, X Series, R Series, Propaq MD, AED Pro, AED 3 BLS |
| Generic name | Automated external defibrillators (non-wearable) |
| Applicant | ZOLL Medical Corporation |
| Product code | MKJ |
| Received date | Apr 17, 2025 |
| Decision date | Aug 28, 2025 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: