# K151246: Aneroid Sphygmomanometer

- Pathway: 510(k) (Traditional)
- Applicant: Jiaxing Zhongfa Medical Products Co., Ltd.
- Decided: Jun 30, 2015 after 50 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: 2 generations back to K060871 (2006). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K092245: Aneroid Sphygmomanometer with Stethoscope, Model LD-100, Honsun (Nantong) Co., Ltd. (2009) Summary page 6.

## Indications for use
The Aneroid Sphygmomanometer is a non-automated, mechanical blood pressure monitor that is used for the indirect measurement (non-invasive) and display of arterial blood pressure. It can be used by professionals as well as trained individual users over age 18 at hospitals or at home to monitor both systolic and diastolic pressure.

Source page: https://510kreport.com/device/K151246
Methodology: https://510kreport.com/methodology