FDA 510(k) Applications Submitted by SYLPHAR N.V.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K132426 | 08/05/2013 | SYLPHAR REMESENSE SENSITIVITY RELIEF STRIPS | SYLPHAR N.V. |
| K122708 | 09/04/2012 | REMESENSE FOR SENSITIVE TEETH | SYLPHAR N.V. |
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