Shenzhen Mericonn 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 |
|---|
| K212300 | Pulse Oximeter | February 25, 2022 |
| K212084 | Fetal Doppler | November 3, 2021 |