WRISTWATCH BPM BLOOD PRESSURE MONITOR, MODEL KP-6120— 510(k) K002665

Substantially Equivalent

K-Jump Health Co., Ltd.

FDA 510(k) clearance K002665 for WRISTWATCH BPM BLOOD PRESSURE MONITOR, MODEL KP-6120, Substantially Equivalent on 2001-03-19. Applicant: K-Jump Health Co., Ltd..

Clearance details

Applicant: K-Jump Health Co., Ltd.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2000-08-25
Decision date: 2001-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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.