Fetal Doppler
K-Number: K212084 · 2021-11-03
Decision Date2021-11-03
Product CodeKNG
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
Fetal Doppler is a medical device manufactured by Shenzhen Mericonn Technology Co., Ltd.. It received FDA 510(k) clearance on 2021-11-03 under approval number K212084. The device is classified under product code KNG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Fetal Doppler?
Fetal Doppler is a medical device that received FDA 510(k) clearance on 2021-11-03. It is manufactured by Shenzhen Mericonn Technology Co., Ltd.. The 510(k) number is K212084.
When was Fetal Doppler approved by the FDA?
Fetal Doppler received FDA 510(k) clearance on 2021-11-03, under approval number K212084.
What company makes Fetal Doppler?
Fetal Doppler is manufactured by Shenzhen Mericonn Technology Co., Ltd..
What is the FDA product code for Fetal Doppler?
The FDA product code for Fetal Doppler is KNG.
Related Clinical Trials
Other Devices by Shenzhen Mericonn Technology Co., Ltd.
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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.