# K111830: Fully Automatic Electronic Blood Pressure Monitor Model KD-7902BTJ, Fully Automatic Electronic Blood Pressure Monitor MO

- Pathway: 510(k) (Special)
- Applicant: Andon Health Co, Ltd.
- Decided: Dec 9, 2011 after 164 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 K001671 (2000). 12 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K093452: Fully Automatic Electronic Blood Pressure Monitor Model KD-571, KD-7971, Andon Health Co, Ltd. (2009) Summary page 3.
- K102906: Fully Automatic Electronic Blood Pressure Monitor, Andon Health Co, Ltd. (2010) Summary page 2.

## Most influential descendants
- K160563: Fully Automatic Electronic Blood Pressure Monitor (2016), 0 descendants of its own

## Indications for use
KD-7902BTJ, KD-7963NJ, KD-7971J and KD-7966 Fully Automatic Electronic Blood Pressure Monitor are for use by medical professionals or at home and are 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/K111830
Methodology: https://510kreport.com/methodology