# K102825: Blood Pressure Cuff

- Pathway: 510(k) (Traditional)
- Applicant: APK Technology Co., Ltd.
- Decided: Mar 2, 2011 after 154 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: 3 generations back to K010686 (2001). 3 ancestors in all.
23 later devices descend from it; 3 cite 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)
- K062238: Tytan Blood Pressure Cuff, Tytan Medical Corp. (2006) Summary page 3.

## Cited in the summary but kept off the family tree
- K080850: Darco Headless Compression Screw, Wrightmedicaltechnologyinc (2008). Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree

## Most influential descendants
- 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
- K160981: Patient Monitor (2016), 8 descendants of its own
- K192514: Patient Monitor (2020), 6 descendants of its own

## Indications for use
Blood Pressure Cuffs, include reusable and disposable, are intended to be wrapped on the upper arm and used with a non-invasive blood pressure monitor system to determine blood parameters on neonate, pediatric and adult patients.

Source page: https://510kreport.com/device/K102825
Methodology: https://510kreport.com/methodology