A&D MEDICAL UA-767F AND UA-767FAC DIGITAL BLOOD PRESSURE MONITOR— 510(k) K141201

Substantially Equivalent

A & D Co., Ltd.

FDA 510(k) clearance K141201 for A&D MEDICAL UA-767F AND UA-767FAC DIGITAL BLOOD PRESSURE MONITOR, Substantially Equivalent on 2014-10-08. Applicant: A & D Co., Ltd..

Clearance details

Applicant: A & D Co., Ltd.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2014-05-09
Decision date: 2014-10-08
Decision: Substantially Equivalent
Clearance type: Special
Location: San Jose, CA, 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.