Shanghai Berry Electronic Tech Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K250837 | Pulse Oximeter | September 25, 2025 |
| K172141 | Pulse Oximeter | April 4, 2018 |
| K142687 | Pulse Oximeter | April 13, 2015 |