Jolife AB
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| 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 |
| 510(k) | K090422 | LUCAS 2 | DRM | 2009-06-17 | View |
| 510(k) | K062401 | MODIFICATION TO LUCAS | DRM | 2006-09-28 | View |
| 510(k) | K053403 | LUCAS | DRM | 2006-02-01 | View |
No matching devices.
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