# K051539: Tricot Blood Pressure Cuff

- Pathway: 510(k) (Traditional)
- Applicant: Ya Horng Electronic Co., Ltd.
- Decided: Aug 5, 2005 after 56 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: 1 generation back to K010686 (2001). 1 ancestor in all.
25 later devices descend from it; 1 cites it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K010686: KTJ-20C Blood Pressure Cuff, Model KTJ-20C, Golden Horse Medical Equipment (Wuxi) Co., Ltd. (2001) Summary page 1.

## Most influential descendants
- K062238: Tytan Blood Pressure Cuff (2006), 24 descendants of its own
- K102825: Blood Pressure Cuff (2011), 23 descendants of its own
- K113623: Patient Monitor (2012), 15 descendants of its own
- K131971: IM60/IM70 Patient Monitor (2014), 14 descendants of its own
- K120173: Patient Monitor (2012), 10 descendants of its own

## Indications for use
The TRICOT blood pressure cuff is used in conjunction with non-invasive blood pressure measurement systems by personnel properly trained. The device is non-sterile and is intended as a reusable multi-patient device for measuring one's blood pressure. It is available in child through large adult sizes.

Source page: https://510kreport.com/device/K051539
Methodology: https://510kreport.com/methodology