FDA 510(k) Applications Submitted by ISABELLE DURAND
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K162067 | 07/26/2016 | VX130 Ophthalmic Diagnostic Device | LUNEAU SAS |
| K143086 | 10/27/2014 | VX120 Ophthalmic Diagnostic Device | LUNEAU SAS |
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