FDA 510(k) Applications Submitted by CEFAR MEDICAL AB
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K030403 | 02/06/2003 | CEFAR REHAB 2 AND REHAB 2 PRO | CEFAR MEDICAL AB |
| K020803 | 03/12/2002 | CEFAR MEDICAL AB CEFAR PRIMO | CEFAR MEDICAL AB |
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