Fetal Doppler
K-Number: K211940 · 2022-01-07
Decision Date2022-01-07
Product CodeKNG
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
Fetal Doppler is a medical device manufactured by Shenzhen Taikang Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2022-01-07 under approval number K211940. 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 2022-01-07. It is manufactured by Shenzhen Taikang Medical Equipment Co., Ltd.. The 510(k) number is K211940.
When was Fetal Doppler approved by the FDA?
Fetal Doppler received FDA 510(k) clearance on 2022-01-07, under approval number K211940.
What company makes Fetal Doppler?
Fetal Doppler is manufactured by Shenzhen Taikang Medical Equipment Co., Ltd..
What is the FDA product code for Fetal Doppler?
The FDA product code for Fetal Doppler is KNG.
Related Clinical Trials
Related Devices (Code: KNG)
K153475SD5 & SD6 Ultrasonic Tabletop DopplerEdan Instruments, Inc.
K182190Fetal DopplerShenzhen AOJ Medical Technology Co., Ltd.
K180419Ultrasonic Doppler (Model YM-2T8)Shenzhen Imdk Medical Technology Co., Ltd.
K172780SD1 Ultrasonic Pocket DopplerEdan Instruments, Inc.
K191110HeraBEAT USHeramed, Ltd.
K182526Fetal Doppler (Models: FD-231B, FD-231D, FD-640B, FD-640D, FD-200B, FD-200D, FD-591B, and FD-591D)Vcomin Technology Limited
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.