Yikang Endotracheal Tube
K-Number: K190213 · 2019-09-06
Decision Date2019-09-06
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
Yikang Endotracheal Tube is a medical device manufactured by Jiangxi Yikang Medical Instrument Group Co., Ltd.. It received FDA 510(k) clearance on 2019-09-06 under approval number K190213. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Yikang Endotracheal Tube?
Yikang Endotracheal Tube is a medical device that received FDA 510(k) clearance on 2019-09-06. It is manufactured by Jiangxi Yikang Medical Instrument Group Co., Ltd.. The 510(k) number is K190213.
When was Yikang Endotracheal Tube approved by the FDA?
Yikang Endotracheal Tube received FDA 510(k) clearance on 2019-09-06, under approval number K190213.
What company makes Yikang Endotracheal Tube?
Yikang Endotracheal Tube is manufactured by Jiangxi Yikang Medical Instrument Group Co., Ltd..
What is the FDA product code for Yikang Endotracheal Tube?
The FDA product code for Yikang Endotracheal Tube is BTR.
Other Devices by Jiangxi Yikang Medical Instrument Group 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.