# K032837: HL888BM

- Pathway: 510(k) (Special)
- Applicant: Health & Life Co., Ltd.
- Decided: Oct 10, 2003 after 29 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices 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.

## Most influential descendants
- K093823: Full Automatic (Nibp) Blood Pressure Monitor, Model HL888V, Full Automatic (Nibp) Blood Pressure Monitor, Model HL868JM (2010), 0 descendants of its own

## Indications for use
Manual inflate type blood pressure monitor for measurement of human's systolic, diastolic blood pressure and heart rate using the oscillometric method. All values can be read out in an LCD panel. The intended use of this over-the counter device is for adult patients whose arm circumference is between 24-32cm (approx. 9.4" to 12.6").

Source page: https://510kreport.com/device/K032837
Methodology: https://510kreport.com/methodology