# K083317: Fully Automatic Electronic Blood Pressure Monitor, Model KD-5902

- Pathway: 510(k) (Special)
- Applicant: Andon Health Co, Ltd.
- Decided: Jan 29, 2009 after 80 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.
17 later devices descend from it; 5 cite it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070828: KD-595 Fully Automatic Electronic Blood Pressure Monitor, Kodon (Tianjin)Electronic&Electrical Apparatus Co., (2007) Summary page 1.

## Most influential descendants
- K090768: Fully Automatic Electronic Blood Pressure Monitor, Models KD 5901, KD-7909, (2009), 5 descendants of its own
- K091737: Fully Automatic Electronic Blood Pressure Monitor, Models: KD-5917, KD-5915, KD-5031 (2009), 4 descendants of its own
- K090771: Fully Automatic Electronc Blood Pressure Monitor, Model, KD-5962 (2009), 4 descendants of its own
- K092045: Fully Automatic Electronic Blood Pressure Monitor, Models KD-738 and KD-739 (2009), 3 descendants of its own
- K093452: Fully Automatic Electronic Blood Pressure Monitor Model KD-571, KD-7971 (2009), 2 descendants of its own

## Indications for use
KD-5902 Fully Automatic 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 upper arm. The cuff circumference is limit(d to 22cm-48cm.

Source page: https://510kreport.com/device/K083317
Methodology: https://510kreport.com/methodology