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FDA 510(k)

Electronic Sphygmomanometers, Model: X1, X2, X5, X6, X7,X8, X11)

K-Number: K221040 · 2022-08-31

Decision Date2022-08-31
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Electronic Sphygmomanometers, Model: X1, X2, X5, X6, X7,X8, X11) is a medical device manufactured by Jiangxi Aicare Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-08-31 under approval number K221040. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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.

Related Clinical Trials

Other Devices by Jiangxi Aicare Medical Technology Co., Ltd.

Related Devices (Code: DXN)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.