# K110018: Fully Automatic Electronic Blood Pressure Monitor

- Pathway: 510(k) (Special)
- Applicant: Andon Health Co, Ltd.
- Decided: Mar 15, 2011 after 71 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 K001670 (2000). 11 ancestors in all.
No later device cites it as a predicate yet.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091997: Fully Automatic Electronic Blood Pressure Monitor, Model KD-7962, Andon Health Co, Ltd. (2009) Summary page 2.
- K092045: Fully Automatic Electronic Blood Pressure Monitor, Models KD-738 and KD-739, Andon Health Co, Ltd. (2009) Summary page 2.

## Indications for use
KD-734 series, KD-735 series, KD-7908, KD-7908V and KD-792RT Fully Automatic Electronic Blood Pressure Monitor are 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 14cm-25cm.

Source page: https://510kreport.com/device/K110018
Methodology: https://510kreport.com/methodology