# K173024: Non-invasive blood pressure measurement systems

- Pathway: 510(k) (Traditional)
- Applicant: Joytech Healthcare Co., Ltd.
- Decided: Aug 22, 2018 after 328 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.
3 later devices descend from it; 3 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K213189: Wrist-type Fully Automatic Digital Blood Pressure Monitor (2022), 0 descendants of its own
- K200649: Arm-Type Fully Automatic Digital Blood Pressure Monitor (2020), 0 descendants of its own
- K190886: Non-invasive blood pressure measurement systems (2019), 0 descendants of its own

Source page: https://510kreport.com/device/K173024
Methodology: https://510kreport.com/methodology