# K172226: MX40 Release B.07

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems
- Decided: Nov 9, 2017 after 107 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: 28 generations back to K941811 (1994). 169 ancestors in all.
13 later devices descend from it; 2 cite it directly.
0 of 183 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K103646: Intellivue MX40 Patient Monitor, Phillips Medical Systems (2011) Summary page 5.
- K113125: Intellivue MX40 Patient Monitor, Philips Medical Systems (2011) Summary page 7.

## Most influential descendants
- K193391: BeneVision Central Monitoring System (2020), 10 descendants of its own
- K220058: BeneVision Central Monitoring System (2022), 3 descendants of its own
- K223567: CNS-2101 Central Monitor (2023), 2 descendants of its own
- K242750: Central Station (2025), 1 descendant of its own
- K232694: Central Monitoring System (MFM-CMS) (2024), 1 descendant of its own

## Indications for use
The device is intended for monitoring and recording of and to generate alarms for, multiple physiological parameters of adults and pediatrics in a hospital environment and during patient transport inside hospitals. Not intended for home use. Intended for use by health care professionals. Indicated for use by health care professionals whenever there is a need for monitoring the physiological parameters of patients. Intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults and pediatrics in hospital environments and during transport inside hospitals.

Source page: https://510kreport.com/device/K172226
Methodology: https://510kreport.com/methodology