# K030359: KD-726 Memory Wrist Automatic Electronic Blood Pressure Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Kodon (Tianjin)Electronic&Electrical Apparatus Co.,
- Decided: Nov 6, 2003 after 276 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: 1 generation back to K001671 (2000). 1 ancestor in all.
40 later devices descend from it; 4 cite it directly.
0 of 42 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K001671: Ultra Compact Wrist Blood Pressure Monitor with Intellisense, Model Hem-630, Omron Healthcare, Inc. (2000)

## Most influential descendants
- K070826: KD-795 Wrist Measurement Electronic Blood Pressure Monitor (2007), 33 descendants of its own
- K090769: Fully Automatic Electronic Blood Pressure Monitor, Model KD-7961 (2009), 8 descendants of its own
- K091997: Fully Automatic Electronic Blood Pressure Monitor, Model KD-7962 (2009), 7 descendants of its own
- K150430: Arm Blood Pressure Monitor, Wrist Blood Pressure Monitor (2015), 6 descendants of its own
- K102920: Electronic Blood Pressure Monitor (2010), 6 descendants of its own

## Indications for use
The KD-726 Memory Wrist Electronic 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 wrist. The cuff circumference is limited to 6.1023 inches to 9.8425 inches.

Source page: https://510kreport.com/device/K030359
Methodology: https://510kreport.com/methodology