AUTOMATIC BLOOD PRESSURE MONITOR— 510(k) K130925

Substantially Equivalent

Honsun (Nantong) Co., Ltd.

FDA 510(k) clearance K130925 for AUTOMATIC BLOOD PRESSURE MONITOR, Substantially Equivalent on 2013-09-12. Applicant: Honsun (Nantong) Co., Ltd..

Clearance details

Applicant: Honsun (Nantong) Co., Ltd.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2013-04-03
Decision date: 2013-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nantong, Jiangsu, CN

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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, 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.