HOSMAN USB BLOOD PRESSURE MONITOR; WRIST TYPE AND UPPER ARM TYPE— 510(k) K103046

Substantially Equivalent

Hosman International Co., Ltd.

FDA 510(k) clearance K103046 for HOSMAN USB BLOOD PRESSURE MONITOR; WRIST TYPE AND UPPER ARM TYPE, Substantially Equivalent on 2011-01-10. Applicant: Hosman International Co., Ltd..

Clearance details

Applicant: Hosman International Co., Ltd.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2010-10-14
Decision date: 2011-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hsin Chu City, TW

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.