| K-number | DEN230027 |
| Device name | NaviCam ProScan |
| Applicant | Ankon Technologies Co., Ltd. |
| Product code | QZF |
| Device class | Class II |
| Decision date | Dec 12, 2023 |
| Decision | Not Substantially Equivalent |
| Regulation | 876.1540 |
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