Shenzhen Dongjilian Medical Tech 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 |
|---|
| K233536 | Air Compression Recovery System | December 16, 2023 |
| K222206 | Air Compression Leg Massager (Models: S9036C, S9036B and S9036A) | September 30, 2022 |