# K032858: The Philips Intellivue MP40, MP50, MP60, MP70,and MP90 Patient Monitors, Release B.O.

- Pathway: 510(k) (Special)
- Applicant: Philips Medizin Systeme Boblingen GmbH
- Decided: Oct 10, 2003 after 28 days
- Product code: DSI (Detector And Alarm, Arrhythmia)
- 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: 11 generations back to K941811 (1994). 53 ancestors in all.
375 later devices descend from it; 37 cite it directly.
0 of 429 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K001664: Compact Portable Patient Monitor with Wireless Alan, Model Alilent M3000A/M3046A Option J120, Agilent Technologies, Inc. (2000) Summary page 2.
- K021778: Philips Component Compact Monitor, Release a.04, Model #M1275B, Philips Medical Systems (2002) Summary page 2.
- K030038: Philips MP60, MP70 and MP90 Intellivue Patient Monitors with Portal Technology and M3185 Opt C41 Wireless Bedside Adaptr, Philips Medical Systems, Inc. (2003)
- K031481: The Philips Intellivue MP60, MP70, and MP90 Patient Monitors, Release a.20, Philips Medizin Systeme Boblingen GmbH (2003) Summary page 2.

## Most influential descendants
- K040259: Masimo Set Intellivue Pulse Oximeter Module (2004), 312 descendants of its own
- K040304: Philips Intellivue Patient Monitor, Models MP40 & MP50 (2004), 253 descendants of its own
- K041235: Philips MP20, MP30, MP40, MP50. MP60, MP70 and MP90 Intellivue Patient Monitors (2004), 252 descendants of its own
- K042845: The Philips MP20, MP30, MP40, MP50, MP60, MP70, and MP90 Intellivue Patient Monitors (2004), 251 descendants of its own
- K050141: The Philips MP20, MP30, MP40, MP50, MP60, MP70 and MP90 Intellivue Patient Monitors (2005), 250 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. Intended for monitoring, recording and alarming of multiple physiological parameters of adults, pediatrics and neonates in hospital environments. EASI 12-lead ECG is only for use on adult and pediatric patients. ST Segment monitoring is restricted to adult patients only. The transcutaneous gas measurement (tcp02 / tcpC02) is restricted to neonatal patients only.

Source page: https://510kreport.com/device/K032858
Methodology: https://510kreport.com/methodology