Shenzhen Bestman Instrument 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 |
|---|
| K242846 | Doppler FHR Detector (BF-500D+, BF-560) | June 26, 2025 |
| K090510 | DOPPLER FETAL HEARTBEAT RATE DETECTOR | April 29, 2010 |