# K133117: Andon Blood Pressure Cuff

- Pathway: 510(k) (Traditional)
- Applicant: Andon Health Co, Ltd.
- Decided: Mar 4, 2014 after 155 days
- Product code: DXQ (Blood Pressure Cuff)
- Device class: 2
- Regulation: 21 CFR 870.1120
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K010686 (2001). 4 ancestors in all.
4 later devices descend from it; 3 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102825: Blood Pressure Cuff, APK Technology Co., Ltd. (2011) Summary page 1.

## Most influential descendants
- K171889: Reusable Blood Pressure Cuff (2017), 2 descendants of its own
- K233276: Reusable Blood Pressure Cuff (2023), 1 descendant of its own
- K254287: Medline Reusable Blood Pressure Cuff (2026), 0 descendants of its own
- K151810: Bpump Blood Pressure Cuff (2015), 0 descendants of its own

## Indications for use
Blood Pressure Cuffs are intended to be wrapped on the upper arm and used with a non-invasive blood pressure monitor system to complete the measurement of blood parameters on adults.

Source page: https://510kreport.com/device/K133117
Methodology: https://510kreport.com/methodology