Shenzhen Hingmed Medical Instrument Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K251581 | Wearable Ambulatory Blood Pressure Monitor (WBP-02A) | February 13, 2026 |
| K251307 | Clinical Automatic Blood Pressure Monitor (DBP-20,DBP-20i) | January 12, 2026 |
| K231984 | Clinical Automatic Blood Pressure Monitor (DBP-01P,DBP-01HP) | March 26, 2024 |