Guangdong Youkey Medical 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 |
|---|
| K231930 | Digital Ultrasonic Diagnostic Imaging System (Model: F6) | March 22, 2024 |
| K211746 | Pocket Ultrasound System | February 18, 2022 |