Defibtech, LLC
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest Approval2021-11-09
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K211289 | RMU-2000 Automated Chest Compression System | DRM | 2021-11-09 | View |
| PMA | P160032 | Automated external defibrillators (non-wearable) | MKJ | 2018-12-06 | View |
No matching devices.