FDA 510(k)

Doppler FHR Detector (BF-500D+, BF-560)

Número K: K242846 · 2025-06-26

RequerenteShenzhen Bestman Instrument Co., Ltd.

Data da decisão2025-06-26

Código do produtoKNG

Comité consultivoOB

DecisãoSubstantially Equivalent

Resumo do dispositivo

Doppler FHR Detector (BF-500D+, BF-560) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Bestman Instrument Co., Ltd.. It received FDA 510(k) clearance on 2025-06-26 under 510(k) number K242846. The device is classified under product code KNG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Doppler FHR Detector (BF-500D+, BF-560)?

Doppler FHR Detector (BF-500D+, BF-560) is a medical device that received FDA 510(k) clearance on 2025-06-26. The listed applicant is Shenzhen Bestman Instrument Co., Ltd.. The 510(k) number is K242846.

When did Doppler FHR Detector (BF-500D+, BF-560) receive FDA 510(k) clearance?

Doppler FHR Detector (BF-500D+, BF-560) received FDA 510(k) clearance on 2025-06-26, under 510(k) number K242846.

Who is the listed applicant for Doppler FHR Detector (BF-500D+, BF-560)?

The FDA 510(k) record lists Shenzhen Bestman Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Doppler FHR Detector (BF-500D+, BF-560)?

The FDA product code for Doppler FHR Detector (BF-500D+, BF-560) is KNG.

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