Shenzhen Yolanda Technology 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 |
|---|
| K230176 | Upper Arm Blood Pressure Monitor | June 29, 2023 |
| K221211 | Infrared thermometer | September 27, 2022 |
| K221212 | Upper Arm Blood Pressure Monitor | August 26, 2022 |