# K023960: Lidcoplus Hemodynamic Monitor System, Model HM 70

- Pathway: 510(k) (Special)
- Applicant: Lidco, Ltd.
- Decided: Jan 9, 2003 after 41 days
- Product code: DXG (Computer, Diagnostic, Pre-Programmed, Single-Function)
- Device class: 2
- Regulation: 21 CFR 870.1435
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 4 cite it directly.
0 of 8 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
- K181372: Argos (2018), 2 descendants of its own
- K080116: Transonic Costatus Cardiac Output System (2008), 2 descendants of its own
- K113821: Transonic Costatus Cardiac Output System (2012), 1 descendant of its own
- K253092: Argos Infinity (Rev. 1.0) (2026), 0 descendants of its own
- K251275: VitalStream ART Connect; VitalStream-Hemo (2025), 0 descendants of its own

## Indications for use
The LiDCOplus Hemodynamic Monitor is intended for use as a diagnostic aid for the measurement of blood pressure, cardiac output and associated hemodynamic parameters in patients greater than 881b (40kg) in weight.

Source page: https://510kreport.com/device/K023960
Methodology: https://510kreport.com/methodology