# K102906: Fully Automatic Electronic Blood Pressure Monitor

- Pathway: 510(k) (Special)
- Applicant: Andon Health Co, Ltd.
- Decided: Oct 29, 2010 after 28 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
No predicates in its family tree.
19 later devices descend from it; 5 cite it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K162230: Fully Automatic Electronic Blood Pressure Monitor (2016), 6 descendants of its own
- K183534: Fully Automatic Electronic Blood Pressure Monitor (2019), 5 descendants of its own
- K210770: Arm Blood Pressure Monitor, Wireless Blood Pressure Monitor (2021), 4 descendants of its own
- K121372: Fully Automatic Electronic Blood Pressure Monitor (2012), 3 descendants of its own
- K121470: Fully Automatic Wireless Blood Pressure Wrist Monitor (2012), 3 descendants of its own

Source page: https://510kreport.com/device/K102906
Methodology: https://510kreport.com/methodology