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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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