PMA supplement
P160032 S016: Defibtech Automated External Defibrillator (AED) Systems
FDA PMA supplement · Special (Immediate Track) · Defibtech, LLC
Key facts
| Original PMA | P160032 |
|---|---|
| Supplement number | S016 |
| Supplement type | Special (Immediate Track) |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | Defibtech Automated External Defibrillator (AED) Systems |
| Generic name | Automated external defibrillators (non-wearable) |
| Applicant | Defibtech, LLC |
| Product code | MKJ |
| Received date | Jun 16, 2026 |
| Decision date | Jun 25, 2026 |
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: