PMA supplement
P160022 S008: X Series®/Propaq MD device
FDA PMA supplement · Real-Time Process · ZOLL Medical Corporation
Key facts
| Original PMA | P160022 |
|---|---|
| Supplement number | S008 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | X Series®/Propaq MD device |
| Generic name | Automated external defibrillators (non-wearable) |
| Applicant | ZOLL Medical Corporation |
| Product code | MKJ |
| Received date | Oct 1, 2018 |
| Decision date | Dec 16, 2019 |
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: