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Dongguan Kangweile Electronic Technology 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 |
| K230642 | Electronic Blood Pressure Monitor | August 11, 2023 |
| K212171 | Electronic Blood Pressure Monitor | November 1, 2021 |