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. The listed applicant is Jiangxi Aicare Medical Technology Co., Ltd.. The 510(k) number is K221040.
When did Electronic Sphygmomanometers, Model: X1, X2, X5, X6, X7,X8, X11) receive FDA 510(k) clearance?
Electronic Sphygmomanometers, Model: X1, X2, X5, X6, X7,X8, X11) received FDA 510(k) clearance on 2022-08-31, under 510(k) number K221040.
Who is the listed applicant for Electronic Sphygmomanometers, Model: X1, X2, X5, X6, X7,X8, X11)?
The FDA 510(k) record lists Jiangxi Aicare Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Jiangxi Aicare Medical Technology Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: DXN)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
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