# K103268: Omni Express

- Pathway: 510(k) (Special)
- Applicant: Infinium Medical
- Decided: Nov 23, 2010 after 19 days
- Product code: MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms))
- Device class: 2
- Regulation: 21 CFR 870.2300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K021154 (2003). 2 ancestors in all.
5 later devices descend from it; 1 cites 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)
- K101052: Omni Iii Patient Monitor, Infinium Medical (2010) Summary page 2.

## Most influential descendants
- K103737: Omni II Patient Monitor (2011), 4 descendants of its own
- K112329: Omni Patient Monitor (2011), 3 descendants of its own
- K132229: Omni Patent Monitors (2014), 2 descendants of its own
- K153079: Axeo 3 Patient Monitor (2016), 0 descendants of its own
- K142244: Cleo Patient Monitor (2015), 0 descendants of its own

## Indications for use
The purpose and function of the OMNI Express monitor is to monitor ECG, heart rate, NIBP (systolic, diastolic, and mean arterial pressures), SPO2, respiration, and temperature, for adult, neonate and pediatric patients. It may be used as a bedside or portable monitor and be used in all hospitals and hospital-type facilities such as clinics and emergency room facilities.

Source page: https://510kreport.com/device/K103268
Methodology: https://510kreport.com/methodology