# K231310: Electronic Blood Pressure Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Jumper Medical Equipment Co., Ltd.
- Decided: Oct 27, 2023 after 175 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: 3 generations back to K042505 (2005). 3 ancestors in all.
3 later devices descend from it; 3 cite it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K182127: Wrist Blood Pressure Monitor Model BP6100, Omron Healthcare, Inc. (2018) Summary page 4.

## Most influential descendants
- K253126: Wrist Blood Pressure Monitor (XW-05) (2026), 0 descendants of its own
- K253133: Wrist Blood Pressure Monitor (BPM-W1VL) (2026), 0 descendants of its own
- K241634: Wrist Blood Pressure Monitor (XY-W01A, XY-W01B) (2025), 0 descendants of its own

## Indications for use
The Electronic Blood Pressure Monitor is intended to measure the systolic and diastolic blood pressure as well as the pulse rate of adult person via non-invasive oscillometric technique at medical facilities or at home. The intended wrist circumference is 13.5-21.5 cm.

Source page: https://510kreport.com/device/K231310
Methodology: https://510kreport.com/methodology