# K182495: Electronic Blood Pressure Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Jumper Medical Equipment Co., Ltd.
- Decided: Mar 3, 2019 after 173 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 K001670 (2000). 6 ancestors in all.
11 later devices descend from it; 1 cites it directly.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170151: Electronic Blood Pressure Monitor, Shenzhen Pango Electronic Co., Ltd. (2017) Summary page 4.

## Most influential descendants
- K191180: Electronic Blood Pressure Monitor (2019), 10 descendants of its own
- K222125: Arm Blood Pressure Monitor, models AOJ-30A, AOJ-30B, AOJ-30C, AOJ-30D, AOJ-30E, AOJ-30F and AOJ-30G (2022), 4 descendants of its own
- K222994: Arm Blood Pressure Monitor, models AOJ-33A and AOJ-33B (2023), 1 descendant of its own
- K213503: Wrist Blood Pressure Monitor, models AOJ-35A, AOJ-35B, AOJ-35C, AOJ-35D, AOJ-35E (2022), 1 descendant of its own
- K261136: Blood Pressure Monitor (M501,M501A,M502,M502A,M502C,M502D) (2026), 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.

Source page: https://510kreport.com/device/K182495
Methodology: https://510kreport.com/methodology