# K141755: Arm-Type Fully Automatic Digital Blood Pressure Monitor

- Pathway: 510(k) (Special)
- Applicant: Sejoy Electronics & Instruments Co., Ltd.
- Decided: Nov 19, 2014 after 142 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K152687: Arm-Type Fully Automatic Digital Blood Pressure Monitor (2015), 0 descendants of its own

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

Source page: https://510kreport.com/device/K141755
Methodology: https://510kreport.com/methodology