DOPPLER FETAL HEARTBEAT RATE DETECTOR
K-Number: K090510 · 2010-04-29
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Device Summary
Frequently Asked Questions
What is the DOPPLER FETAL HEARTBEAT RATE DETECTOR?
DOPPLER FETAL HEARTBEAT RATE DETECTOR is a medical device that received FDA 510(k) clearance on 2010-04-29. The listed applicant is Shenzhen Bestman Instrument Co., Ltd.. The 510(k) number is K090510.
When did DOPPLER FETAL HEARTBEAT RATE DETECTOR receive FDA 510(k) clearance?
DOPPLER FETAL HEARTBEAT RATE DETECTOR received FDA 510(k) clearance on 2010-04-29, under 510(k) number K090510.
Who is the listed applicant for DOPPLER FETAL HEARTBEAT RATE DETECTOR?
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 FETAL HEARTBEAT RATE DETECTOR?
The FDA product code for DOPPLER FETAL HEARTBEAT RATE DETECTOR is KNG.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Shenzhen Bestman Instrument Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KNG)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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