# K143057: M3290B Philips IntelliVue Information Center iX

- Pathway: 510(k) (Special)
- Applicant: Philips Medical Systems
- Decided: Dec 3, 2014 after 40 days
- Product code: MSX (System, Network And Communication, Physiological Monitors)
- Device class: 2
- Regulation: 21 CFR 870.2300
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 23 generations back to K941811 (1994). 135 ancestors in all.
4 later devices descend from it; 1 cites it directly.
0 of 140 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102495: M3290B Intellivue Information Center Software, Release a.0, Philips Medical Systems (2010) Summary page 5.

## Most influential descendants
- K153702: M3290B Philips IntelliVue Information Center iX (2016), 3 descendants of its own
- K163584: M3290B Philips IntelliVue Information Center iX (2017), 2 descendants of its own
- K183387: M3290B Patient Information Center iX (2019), 0 descendants of its own
- K173203: Athena GTX Device Management Suite (ADMS) Software (2018), 0 descendants of its own

## Recalls of this device
- Jan 3, 2018 · Class II · Z-0776-2018: Once a surveillance station is restarted on January 1, 2018 or later, the station will be unable to perform patient discharge and transfer operations. Any subsequent attempt to perform these operation

## 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/K143057
Methodology: https://510kreport.com/methodology