# K141201: A&D Medical UA-767F and UA-767FAC Digital Blood Pressure Monitor

- Pathway: 510(k) (Special)
- Applicant: A & D Co., Ltd.
- Decided: Oct 8, 2014 after 152 days
- Product code: DXN (System, Measurement, Blood-Pressure, Non-Invasive)
- Device class: 2
- Regulation: 21 CFR 870.1130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K982481 (1998). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K043217: A&D Medical UA-767PBT Digital Blood Pressure Monitor, A&D Engineering, Inc. (2005) Summary page 4.
- K111686: A & D Medical UA-1000 Family Dagital Blood Pressure Monitors, A&D Company, Ltd. (2011) Summary page 4.

## Indications for use
The UA-767F and UA-767FAC are designed to be used by users who are older than twelve (12) years at home or clinics to monitor their blood pressure (systolic and diastolic) and pulse rate. The arm circumference range shall be between 8.7 inches (22.0 cm) and 17.7 inches (45.0 cm).

Source page: https://510kreport.com/device/K141201
Methodology: https://510kreport.com/methodology