Wrist Blood Pressure Monitor (5 models)— 510(k) K233799

Substantially Equivalent

Shenzhen Yuezhongxing Technology Co., Ltd.

FDA 510(k) clearance K233799 for Wrist Blood Pressure Monitor (5 models), Substantially Equivalent on 2024-03-15. Applicant: Shenzhen Yuezhongxing Technology Co., Ltd.. Device class: 2.

Clearance details

Device name as filed
Wrist Blood Pressure Monitor (222); Wrist Blood Pressure Monitor (222BT); Wrist Blood Pressure Monitor (W1681BL); Wrist Blood Pressure Monitor (W1681BT); Wrist Blood Pressure Monitor (W1681R)
Applicant
Shenzhen Yuezhongxing Technology Co., Ltd.
Product code
Code DXN
Device class
Class 2
Regulation
21 CFR 870.1130
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Shenzhen, CN
Download summary PDFView on FDA.gov ↗

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Adverse events under product code DXN

product code DXN
Death
3
Injury
169
Malfunction
1,019
Other
2
Total
1,193

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.