# K060835: HL888SF

- Pathway: 510(k) (Special)
- Applicant: Health & Life Co., Ltd.
- Decided: Apr 21, 2006 after 25 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.
15 later devices descend from it; 1 cites it directly.
0 of 16 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
- K092161: Full Automatic (Nibp) Blood Pressure Monitor, Model HL868BF (2009), 14 descendants of its own
- K093831: Fully Automatic (Nibp) Blood Pressure Monitor, Model HL868RT (2010), 12 descendants of its own
- K131121: Full Automatic (Nibp) Blood Pressure Monitor (2013), 9 descendants of its own
- K113238: Full Automatic (Nibp) Blood Pressue Monitor (2012), 9 descendants of its own
- K142968: Full Automatic (NIBP) Blood Pressure Monitor (2014), 8 descendants of its own

## Indications for use
Measures automatically human's Systolic, Diastolic blood pressure and heart rate by using the oscillornetric method, All values can be read out in one LCD panel The intended use of this over-the-counter-deviCe is for the over age of 18,

Source page: https://510kreport.com/device/K060835
Methodology: https://510kreport.com/methodology