Jolife AB
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2018-02-08
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K173553 | LUCAS 3 Chest Compression System | DRM | 2018-02-08 | View |
| 510(k) | K161768 | LUCAS 3 Chest Compression System | DRM | 2016-11-09 | View |
No matching devices.