| K-number | K231805 |
| Device name | qXR-LN |
| Applicant | Qure.Ai Technologies |
| Product code | MYN |
| Device class | Class II |
| Decision date | Dec 22, 2023 |
| Decision | Substantially Equivalent |
| Regulation | 892.2070 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov