# K052450: KD-788 Wrist Measurement Electronic Blood Pressure Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Kodon (Tianjin)Electronic&Electrical Apparatus Co.,
- Decided: Feb 28, 2006 after 174 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: 2 generations back to K001671 (2000). 2 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030359: KD-726 Memory Wrist Automatic Electronic Blood Pressure Monitor, Kodon (Tianjin)Electronic&Electrical Apparatus Co., (2003) Summary page 1.

## Most influential descendants
- K123130: Answatch Wrist Monitor Model TS-0411 (2013), 2 descendants of its own
- K213699: CareTaker Monitor App (2022), 0 descendants of its own
- K201914: HRVWatch-Mini Wrist Monitor (2021), 0 descendants of its own

## Indications for use
The KD-788 Wrist Measurement 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/K052450
Methodology: https://510kreport.com/methodology