Ankon Technologies Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| DEN230027 | NaviCam ProScan | December 12, 2023 |
| K221590 | NaviCam Small Bowel Capsule Endoscopy System | December 2, 2022 |