# K130232: Electronic Blood Pressure Monitor for Upper Arm

- Pathway: 510(k) (Abbreviated)
- Applicant: Jinxinbao Electronic Co.,Ltd
- Decided: Sep 17, 2013 after 231 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.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K120554: Arm-Type Fully Automatic Digital Blood Pressure Monitor, Wrist-Type Fully Automatic Digital Blood Pressure Monitor, Sejoy Electronics & Instruments Co., Ltd. (2012) Summary page 1.

## Indications for use
BPA-002 Electronic Blood Pressure Monitor for Upper Arm is Intended to measure systolic and diastolic blood pressures as well as the determination of heart rate by using the oscillometric method. All values can be read out in one LCD panel. It is suitable for adult arm circumference and can be used by medical departments or for home use. However, it shouldn't be used by people who have severe arrhythmia.

Source page: https://510kreport.com/device/K130232
Methodology: https://510kreport.com/methodology