# K884329: Sat-2 Oximeter/Cardiac Output Computer

- Pathway: 510(k) (Traditional)
- Applicant: Baxter Healthcare Corp
- Decided: Dec 16, 1988 after 63 days
- Product code: DQA (Oximeter)
- Device class: 2
- Regulation: 21 CFR 870.2700
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
68 later devices descend from it; 1 cites it directly.
0 of 69 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
- K960614: Somanetics Invos 3100A Cerebral Oximeter (Invos) (1996), 67 descendants of its own
- K051257: Adult Cerebral Oximeter, Model 2040 (2005), 63 descendants of its own
- K073036: Fore-Sight, MC-2000 Series (2008), 59 descendants of its own
- K061960: Fore-Sight Cerebral Oximeter Monitor, Model 2040 (2006), 59 descendants of its own
- K083892: Fore-Sight, Model MC-2000 Series (MC-2000, MC-2010, MC2020, MC2030) (2009), 58 descendants of its own

Source page: https://510kreport.com/device/K884329
Methodology: https://510kreport.com/methodology