# K042853: Full Automatic (Nibp) Blood Pressure Monitor, Models HL888EA, HL888CF, HL888GF and HL888QA

- Pathway: 510(k) (Special)
- Applicant: Health & Life Co., Ltd.
- Decided: Nov 10, 2004 after 26 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
Measure automatically human's systolic, diastolic blood pressure and heart rate using the oscillometric method. All values can be read out in one LCD panel. The intended use of this over-the counter device is for adult patients whose arm circumference is between 24-44cm (approx. 9.4" to 17.5").

Source page: https://510kreport.com/device/K042853
Methodology: https://510kreport.com/methodology