See-Mode Technologies Pte, Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2024-09-09
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K240697 | See-Mode Augmented Reporting Tool, Thyroid (SMART-T) | QDQ | 2024-09-09 | View |
| 510(k) | K201369 | AVA (Augmented Vascular Analysis) | LLZ | 2020-09-16 | View |
No matching devices.