# K243118: Arm Blood Pressure Monitor (model: BPM-A7VL)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Imdk Medical Technology Co., Ltd.
- Decided: Nov 26, 2024 after 57 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 K001670 (2000). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K241129: Upper Arm Electronic Blood Pressure Monitor, Shenzhen Goodlymed Technology Co., Ltd. (2024) Summary page 6.

## Indications for use
Arm Blood Pressure Monitor is intended to measure the blood pressure and pulse rate of person older than twelve (12) years in household or medical facilities.

Source page: https://510kreport.com/device/K243118
Methodology: https://510kreport.com/methodology