WRIST AUTOMATIC BLOOD PRESSURE MONITOR— 510(k) K123800

Substantially Equivalent

Little Doctor Electronic (Nantong)Co.,Ltd

FDA 510(k) clearance K123800 for WRIST AUTOMATIC BLOOD PRESSURE MONITOR, Substantially Equivalent on 2013-05-15. Applicant: Little Doctor Electronic (Nantong)Co.,Ltd.

Clearance details

Applicant: Little Doctor Electronic (Nantong)Co.,Ltd
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2012-12-10
Decision date: 2013-05-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nantong, 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.