Shandong Int Medical Instruments 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 |
|---|
| K244038 | High Pressure Tubing | September 5, 2025 |
| K242143 | Angiography Injector | December 23, 2024 |