Ankon Technologies Co., Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest Approval2023-12-12
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | DEN230027 | NaviCam ProScan | QZF | 2023-12-12 | View |
| 510(k) | K221590 | NaviCam Small Bowel Capsule Endoscopy System | NEZ | 2022-12-02 | View |
No matching devices.