# K872529: Thermodilution Cardiac Output Computer, Mod. Com-2

- Pathway: 510(k) (Traditional)
- Applicant: American Edwards Laboratories
- Decided: Sep 15, 1987 after 81 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.
5 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K051907: Innocor (2006), 4 descendants of its own
- K071911: Cardiopulmonary Exercise Testing Option to Innocor (2007), 3 descendants of its own
- K083879: Innocor Ergospirometry System (INN00010), the Basic Innocor Including Breath-by-Breath System (INN00400), Nibp (INN00500) (2009), 2 descendants of its own
- K190561: NICU V'02 (2020), 0 descendants of its own
- K102047: Lci Option for Innocor (2011), 0 descendants of its own

Source page: https://510kreport.com/device/K872529
Methodology: https://510kreport.com/methodology