FDA 510(k) Applications for Medical Device Product Code "QQU"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K233720 | Luminopia, Inc. | Luminopia | 08/08/2024 |
| K243819 | Luminopia, Inc. | Luminopia | 04/09/2025 |
| DEN210005 | Luminopia, Inc. | Luminopia One | 10/20/2021 |
| K221659 | Luminopia, Inc. | Luminopia One | 11/04/2022 |
| K221375 | NovaSight Ltd. | CureSight-CS100 | 09/29/2022 |
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