FDA 510(k) Applications Submitted by SHENZHEN BESTMAN INSTRUMENT CO., LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090510 | 02/26/2009 | DOPPLER FETAL HEARTBEAT RATE DETECTOR | SHENZHEN BESTMAN INSTRUMENT CO., LTD. |
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