FDA 510(k) Applications Submitted by Jolife AB
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K053403 | 12/06/2005 | LUCAS | JOLIFE AB |
| K090422 | 02/18/2009 | LUCAS 2 | JOLIFE AB |
| K062401 | 08/16/2006 | MODIFICATION TO LUCAS | JOLIFE AB |
| K161768 | 06/27/2016 | LUCAS 3 Chest Compression System | Jolife AB |
| K173553 | 11/16/2017 | LUCAS 3 Chest Compression System | Jolife AB |
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