FDA 510(k) Applications Submitted by JEAN-YVES MIGNOLET
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160237 | 02/01/2016 | Cefaly | CEFALY TECHNOLOGY |
| K171446 | 05/16/2017 | Cefaly Acute | CEFALY Technology |
| K173006 | 09/27/2017 | Cefaly Dual | CEFALY Technology |
| DEN120019 | 12/13/2012 | CEFALY | STX-MED SPRL |
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