# K101449: Intellivue Patient Monitor

- Pathway: 510(k) (Special)
- Applicant: Philips Medizinsysteme Boeblingen GmbH, Cardiac AN
- Decided: Jun 18, 2010 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: 29 generations back to K941811 (1994). 177 ancestors in all.
92 later devices descend from it; 10 cite it directly.
0 of 270 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K021778: Philips Component Compact Monitor, Release a.04, Model #M1275B, Philips Medical Systems (2002) Summary page 2.
- K100939: Intellivue Patient Monitor Model: MP2, MP5, MP5T, MP20, MP30, MP40, MP50, MP60, MP70, MP75, MP80 and MP90, Philips Medizinsysteme Boeblingen GmbH, Cardiac AN (2010) Summary page 2.

## Most influential descendants
- 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
- K120366: Intellivue Patient Monitor (2012), 46 descendants of its own

## Indications for use
Indicated for use by health care professionals whenever there is a need for monitoring the physiological parameters of patients.

Source page: https://510kreport.com/device/K101449
Methodology: https://510kreport.com/methodology