# K002478: S/5 Compact Anesthesia Monitor with S-00A05, S-00A06. L-00A07, L00A08

- Pathway: 510(k) (Traditional)
- Applicant: Datex-Ohmeda, Inc.
- Decided: Oct 5, 2000 after 55 days
- Product code: MHX (Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms))
- Device class: 2
- Regulation: 21 CFR 870.1025
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
86 later devices descend from it; 1 cites it directly.
1 of 87 devices in its family (counting itself) has 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
- K022485: Datex-Ohmeda S/5 Compact Anesthesia Monitor with L-CANE02 and L-CANE02A Software (2002), 85 descendants of its own
- K041790: Datex-Ohmeda S/5 Compact Anesthesia Monitor with L-CANE03 and LCANE03A Software (2004), 84 descendants of its own
- K053193: PM-8000 Express Patient Monitor, Model PM-8000 Express (2006), 48 descendants of its own
- K070791: PM Series Patient Monitors, Models PM-9000 Express and PM-8000 Express (2007), 47 descendants of its own
- K061185: Datex-Ohmeda S/5 Compact Anesthesia Monitor with L-CANE05A and L-CANE05A Software (2006), 34 descendants of its own

Source page: https://510kreport.com/device/K002478
Methodology: https://510kreport.com/methodology