Luneau Sas
2 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| VX130 Ophthalmic Diagnostic Device (K162067) | Luneau Sas | 2017-04-24 |
| VX120 Ophthalmic Diagnostic Device (K143086) | Luneau Sas | 2015-06-01 |
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