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.
K242846 09/20/2024 Doppler FHR Detector (BF-500D+, BF-560) Shenzhen Bestman Instrument Co., Ltd.


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