Wrist Blood Pressure Monitor (XW-05)

FDA 510(k) K253126 · Shenzhen Ziqing Medical Equipment Co., Ltd.

Substantially Equivalent

510(k) numberK253126

Submission

Device name
Wrist Blood Pressure Monitor (XW-05)
Applicant
Shenzhen Ziqing Medical Equipment Co., Ltd.
Shenzhen, CN
Received
September 25, 2025
Decision date
June 18, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DXN – System, Measurement, Blood-Pressure, Non-Invasive
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1130
Specialty
Cardiovascular

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K253425Arm-type Fully Automatic Digital Blood Pressure Monitor…DXN · Traditional Joytech Healthcare Co. , Ltd.08/13/2026SE
K261136Blood Pressure Monitor (M501,M501A,M502,M502A,M502C,M502D)DXN · Traditional Guangzhou Daxin Health Technology Co., Ltd.07/23/2026SE
K261082Microlife Wrist Blood Pressure Monitor , (Model BPHJG5-G)DXN · Traditional Microlife Corporation07/23/2026SE
K260693VicorderCS (VCS-SYS-1100)DXN · Traditional 80 Beats Medical GmbH06/16/2026SE
K253059Tournicare ARMA Automatic Blood Pressure Monitor (ARMA-08)DXN · Traditional Tournicare Pty, Ltd.06/15/2026SE

More from Tournicare Pty, Ltd.

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K253124Upper arm electronic blood pressure monitor (XB-01)DXN · Traditional 06/03/2026SE

Questions and answers

When was Wrist Blood Pressure Monitor (XW-05) cleared by the FDA?

Wrist Blood Pressure Monitor (XW-05) (K253126) received a 510(k) decision of Substantially Equivalent on June 18, 2026, 266 days after the submission was received.

What is the product code of K253126?

The FDA product code is DXN – System, Measurement, Blood-Pressure, Non-Invasive, a Class II (moderate risk) device regulated under 21 CFR 870.1130.