FDA 510(k) Applications Submitted by Jean Bigoney
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K100749 | 03/16/2010 | FREQUENCER MODEL V2X | DYMEDSO INC. |
| K103176 | 10/28/2010 | FREQUENCER | DYMEDSO INC. |
| K063645 | 12/07/2006 | FREQUENCER, MODEL 1001 | DYMEDSO INC. |
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