# K031403: M3290A Intellivue Information Center Software Release E.1

- Pathway: 510(k) (Special)
- Applicant: Philips Medical Systems, Inc.
- Decided: May 30, 2003 after 25 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: 1 generation back to K011093 (2001). 1 ancestor in all.
263 later devices descend from it; 7 cite it directly.
0 of 265 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011093: Agilent Information Center Software for M3150,M3151,M3153 and M3154, Agilent Technologies, Inc. (2001) Summary page 1.

## Most influential descendants
- K040357: M3290A Intellivue Information Center Software Release F.O and the M4840A Telemetry Monitoring System II (2004), 260 descendants of its own
- K041235: Philips MP20, MP30, MP40, MP50. MP60, MP70 and MP90 Intellivue Patient Monitors (2004), 252 descendants of its own
- K042845: The Philips MP20, MP30, MP40, MP50, MP60, MP70, and MP90 Intellivue Patient Monitors (2004), 251 descendants of its own
- K050141: The Philips MP20, MP30, MP40, MP50, MP60, MP70 and MP90 Intellivue Patient Monitors (2005), 250 descendants of its own
- K050762: Philips Intellivue Patient Monitor, Models MP20, MP30, MP40, MP50, MP60, MP70 and MP90 (2005), 249 descendants of its own

## Indications for use
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/K031403
Methodology: https://510kreport.com/methodology