# K163683: A&D Medical UA-1200BLE UltraConnect Digital Blood Pressure Monitor

- Pathway: 510(k) (Special)
- Applicant: A&D Company, Ltd.
- Decided: May 3, 2017 after 126 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: 6 generations back to K982481 (1998). 8 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141160: A&D Medical UA-651 Digital Blood Pressure Monitor, A & D Co., Ltd. (2014) Summary page 4.
- K043217: A&D Medical UA-767PBT Digital Blood Pressure Monitor, A&D Engineering, Inc. (2005) Summary page 4.

## Most influential descendants
- K231984: Clinical Automatic Blood Pressure Monitor (DBP-01P,DBP-01HP) (2024), 1 descendant of its own
- K251307: Clinical Automatic Blood Pressure Monitor (DBP-20,DBP-20i) (2026), 0 descendants of its own

## Indications for use
Measure blood pressure (systolic and diastolic) and pulse rate.

Source page: https://510kreport.com/device/K163683
Methodology: https://510kreport.com/methodology