# K905140: Satlite Plus Pulse Oximeter

- Pathway: 510(k) (Traditional)
- Applicant: Datex Division Instrumentarium Corp.
- Decided: May 28, 1991 after 194 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.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K990082: Epic SPO2 Finger Sensor, Model E403-09, E412-09 and Epic Oximeter Cable, Model E710-09 (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K905140
Methodology: https://510kreport.com/methodology