# K241129: Upper Arm Electronic Blood Pressure Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Goodlymed Technology Co., Ltd.
- Decided: Jul 3, 2024 after 70 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: 2 generations back to K001670 (2000). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K160019: U80 Series Upper Arm Electronic Blood Pressure Monitor, Shenzhen Urion Technology Co., Ltd. (2016) Summary page 5.

## Most influential descendants
- K243118: Arm Blood Pressure Monitor (model: BPM-A7VL) (2024), 0 descendants of its own

## Indications for use
Upper Arm Electronic Blood Pressure Monitor is intended for used by a person older than twelve (12) years to measure the systolic and diastolic blood pressure and pulse rate.

Source page: https://510kreport.com/device/K241129
Methodology: https://510kreport.com/methodology