Electronic Sphygmomanometers (ZH-X9, ZH-X12, ZH-X16, ZH-X17, ZH-X18, ZH-X19, ZH-X23, ZH-X24)— 510(k) K250185

Substantially Equivalent

Jiangxi Aicare Medical Technology Co., Ltd.

FDA 510(k) clearance K250185 for Electronic Sphygmomanometers (ZH-X9, ZH-X12, ZH-X16, ZH-X17, ZH-X18, ZH-X19, ZH-X23, ZH-X24), Substantially Equivalent on 2025-07-14. Applicant: Jiangxi Aicare Medical Technology Co., Ltd..

Clearance details

Applicant: Jiangxi Aicare Medical Technology Co., Ltd.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2025-01-22
Decision date: 2025-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fuzhou City, CN

Download summary PDF View on FDA.gov ↗

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, 2020-01-01 through 2026-04-23. 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.