# K072070: Philips MP2 and X2 Intellivue Patient Monitors

- Pathway: 510(k) (Special)
- Applicant: Philips Medizinsysteme Boeblingen GmbH, Cardiac AN
- Decided: Aug 10, 2007 after 11 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: 26 generations back to K941811 (1994). 171 ancestors in all.
119 later devices descend from it; 14 cite it directly.
0 of 291 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062392: Philips MP5 Intellivue Patient Monitor, Philips Medizin Systeme Boeblingen GmbH (2006) Summary page 2.
- K063725: MP5 Intellivue Patient Monitor, Philips Medizinsysteme Boeblingen GmbH, Cardiac AN (2007) Summary page 2.
- K071426: MP2, X2, MP5, MP20, MP30, MP40, MP50, MP60, MP70, MP80, and MP90  Intellivue Patient Monitors, Philips Medizinsysteme Boeblingen GmbH, Cardiac AN (2007) Summary page 2.

## Most influential descendants
- K102562: Intellivue Patient Monitor, Models MP2, X2, MP5, MP5T, MP20, MP30, MP40, MP50, MP60, MP70, MP80, MP90, & MX800 (2010), 103 descendants of its own
- K110622: Intellivue Patient Monitor (2011), 90 descendants of its own
- K110474: Philips Intellivue TCG10 (2011), 84 descendants of its own
- K113657: Intellivue Patient Monitor (2012), 81 descendants of its own
- K113441: Physiological Monitor, Patient Monitor (2012), 78 descendants of its own

## Indications for use
Indicated for use by health care professionals whenever there is a need for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics and neonates in a hospital environment and during patient transport inside and outside of hospitals.

Source page: https://510kreport.com/device/K072070
Methodology: https://510kreport.com/methodology