WRIST BLOOD PRESSURE MONITOR, MODEL WS-1100/WS-1100PV— 510(k) K080177

Substantially Equivalent

Nihon Seimitsu Sokki Co., Ltd.

FDA 510(k) clearance K080177 for WRIST BLOOD PRESSURE MONITOR, MODEL WS-1100/WS-1100PV, Substantially Equivalent on 2008-05-09. Applicant: Nihon Seimitsu Sokki Co., Ltd..

Clearance details

Applicant: Nihon Seimitsu Sokki Co., Ltd.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2008-01-24
Decision date: 2008-05-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tachikawa-Shi, Tokyo, JP

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.