FDA 510(k) Applications Submitted by VIVOXID LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K070055 | 01/04/2007 | BONALIVE GRANULES AND BONALIVE PLATES | VIVOXID LTD. |
| K071199 | 04/30/2007 | BONALIVE GRANULES | VIVOXID LTD. |
| K071937 | 07/13/2007 | BONALIVE GRANULES AND BONALIVE PLATES | VIVOXID LTD. |
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