# K180017: MX40 Release C.01

- Pathway: 510(k) (Special)
- Applicant: Philips Medical Systems
- Decided: Jul 24, 2018 after 203 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). 170 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 172 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K172226: MX40 Release B.07, Philips Medical Systems (2017) Summary page 5.

## Most influential descendants
- K242962: Telemetry Monitor 5500 Release 4.0 (867232) (2025), 0 descendants 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/K180017
Methodology: https://510kreport.com/methodology