Huger Medical Instrument 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 |
|---|
| K241639 | Single-use Video Ureterorenoscope (SVU-220US) | July 1, 2024 |
| K230475 | Medical Video Endoscope System | November 3, 2023 |