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Suzhou Minhua Medical Apparatus Supplies Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K241096 | Venera 608 Deep Vein Thrombosis (DVT) Prevention System | January 15, 2025 |
| K233276 | Reusable Blood Pressure Cuff | December 21, 2023 |
| K180389 | Venera 508 Deep Vein Thrombosis (DVT) Prevention System | June 29, 2018 |
| K171889 | Reusable Blood Pressure Cuff | December 19, 2017 |