# K060729: Full Automatic (Nibp) Blood Pressure Monitor, Model HL168FV

- Pathway: 510(k) (Special)
- Applicant: Health & Life Co., Ltd.
- Decided: Apr 12, 2006 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K092163: Full Automatic (Nibp) Blood Pressure Monitor, Model HL168KB (2009), 1 descendant of its own
- K113239: Full Automatic (Nibp) Blood Pressure Monitor (Model HL168KF) (2012), 0 descendants of its own

## Indications for use
Measures automatically human's Systolic, Diastolic blood pressure and heart rate by 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 over the age of 18.

Source page: https://510kreport.com/device/K060729
Methodology: https://510kreport.com/methodology