Zhejiang Soudon Medical Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K232450 | Disposable Hemostatic Clips | January 26, 2024 |
| K232442 | Disposable Endoscope Injection Needles | November 9, 2023 |
| K232476 | Disposable Sphincterotome | November 7, 2023 |