Electronic Sphygmomanometers, Model: X1, X2, X5, X6, X7,X8, X11)
K-Number: K221040 · 2022-08-31
Device Summary
Frequently Asked Questions
What is the Electronic Sphygmomanometers, Model: X1, X2, X5, X6, X7,X8, X11)?
Electronic Sphygmomanometers, Model: X1, X2, X5, X6, X7,X8, X11) is a medical device that received FDA 510(k) clearance on 2022-08-31. It is manufactured by Jiangxi Aicare Medical Technology Co., Ltd.. The 510(k) number is K221040.
When was Electronic Sphygmomanometers, Model: X1, X2, X5, X6, X7,X8, X11) approved by the FDA?
Electronic Sphygmomanometers, Model: X1, X2, X5, X6, X7,X8, X11) received FDA 510(k) clearance on 2022-08-31, under approval number K221040.
What company makes Electronic Sphygmomanometers, Model: X1, X2, X5, X6, X7,X8, X11)?
Electronic Sphygmomanometers, Model: X1, X2, X5, X6, X7,X8, X11) is manufactured by Jiangxi Aicare Medical Technology Co., Ltd..
What is the FDA product code for Electronic Sphygmomanometers, Model: X1, X2, X5, X6, X7,X8, X11)?
The FDA product code for Electronic Sphygmomanometers, Model: X1, X2, X5, X6, X7,X8, X11) is DXN.
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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.