FDA 510(k) Applications Submitted by VIVI S.R.L.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K120318 | 02/02/2012 | VIVI ERGON-X HF | VIVI S.R.L. |
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FDA 510(k) Applications Submitted by VIVI S.R.L.
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