# K120672: KD-936 Fully Automatic Wireless Blood Pressure Monitor

- Pathway: 510(k) (Special)
- Applicant: Andon Health Co, Ltd.
- Decided: Jun 1, 2012 after 88 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: 7 generations back to K001670 (2000). 7 ancestors in all.
27 later devices descend from it; 6 cite it directly.
0 of 35 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102939: Fully Automatic Electronic Blood Pressure Monitor Model KD-931, Andon Health Co, Ltd. (2011) Summary page 1.

## Most influential descendants
- K141984: Fully Automatic Electronic Blood Pressure Monitor (2015), 13 descendants of its own
- K140067: Qardioarm (2014), 8 descendants of its own
- K150430: Arm Blood Pressure Monitor, Wrist Blood Pressure Monitor (2015), 6 descendants of its own
- K162668: Fully Automatic Electronic Blood Pressure Monitor (2017), 5 descendants of its own
- K210770: Arm Blood Pressure Monitor, Wireless Blood Pressure Monitor (2021), 4 descendants of its own

## Indications for use
KD-936 Fully Automatic Wireless Blood Pressure Monitor is for use by medical professionals or at home and is a non-invasive blood pressure measurement system intended to measure the diastolic and systolic blood pressures and pulse rate of an adult individual by using a non-invasive technique in which an inflatable cuff is wrapped around the upper arm. The cuff circumference is limited to 22cm-48cm.

Source page: https://510kreport.com/device/K120672
Methodology: https://510kreport.com/methodology