Defibtech, LLC
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2026-07-24
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| PMA | P160032 | Automated external defibrillators (non-wearable) | MKJ | 2026-07-24 | View |
| 510(k) | K211289 | RMU-2000 Automated Chest Compression System | DRM | 2021-11-09 | View |
No matching devices.