# K050742: M3290A Intellivue Information Center Software Release G.00

- Pathway: 510(k) (Special)
- Applicant: Philips Medical Systems
- Decided: Apr 5, 2005 after 14 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
Longest line of descent: 2 generations back to K011093 (2001). 2 ancestors in all.
16 later devices descend from it; 5 cite it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K031403: M3290A Intellivue Information Center Software Release E.1, Philips Medical Systems, Inc. (2003) Summary page 1.

## Cited in the summary but kept off the family tree
- E011093: IntelliVue Information Center Software. Number could not be read Summary page 1.

## Most influential descendants
- K062271: M3290A Intellivue Information Center Software, Release J.00 (for M3140, M3145, M3150, M3151, M3154, M3155, M3169, M3170) (2006), 9 descendants of its own
- K081983: M3290A Intellivue Information Center Software, Release 1.00 (2008), 8 descendants of its own
- K102495: M3290B Intellivue Information Center Software, Release a.0 (2010), 7 descendants of its own
- K143057: M3290B Philips IntelliVue Information Center iX (2014), 4 descendants of its own
- K100420: Philips Obtracevue Model SW Rev. G.00 (2010), 4 descendants of its own

## Indications for use
Indicated for central monitoring of multiple adult, pediatric, and neonatal patients; and where the clinician decides to monitor cardiac arrhythmia of adult, pediatric, and neonatal patients and/or ST segment of adult patients to gain information for treatment, to monitor adequacy of treatment, or to exclude causes of symptoms.

Source page: https://510kreport.com/device/K050742
Methodology: https://510kreport.com/methodology