# K042845: The Philips MP20, MP30, MP40, MP50, MP60, MP70, and MP90 Intellivue Patient Monitors

- Pathway: 510(k) (Special)
- Applicant: Philips Medizin Systeme Boblingen GmbH
- Decided: Nov 12, 2004 after 28 days
- Product code: MSX (System, Network And Communication, Physiological Monitors)
- Device class: 2
- Regulation: 21 CFR 870.2300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 14 generations back to K941811 (1994). 80 ancestors in all.
251 later devices descend from it; 29 cite it directly.
0 of 332 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K014159: Phillips M1175A/76A/77A Component Monitoring System; Phillips V24/V26 Patient Monitor, Philips Medical Systems, Inc. (2002) Summary page 2.
- K021778: Philips Component Compact Monitor, Release a.04, Model #M1275B, Philips Medical Systems (2002) Summary page 2.
- K032858: The Philips Intellivue MP40, MP50, MP60, MP70,and MP90 Patient Monitors, Release B.O., Philips Medizin Systeme Boblingen GmbH (2003) Summary page 2.
- K040357: M3290A Intellivue Information Center Software Release F.O and the M4840A Telemetry Monitoring System II, Philips Medical Systems, Inc. (2004) Summary page 2.
- K041235: Philips MP20, MP30, MP40, MP50. MP60, MP70 and MP90 Intellivue Patient Monitors, Philips Medizin Systeme Boeblingen GmbH (2004) Summary page 2.

## Cited in the summary but kept off the family tree
- K040334: Navigus Passive Probe, Model NP-1000, Image-Guided Neurologics, Inc. (2004). Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree
- K040183: BISX, Aspect Medical Systems, Inc. (2004). Our reading of the summary gave K040183, FDA’s number for BISX (Aspect Medical Systems, Inc.). Its FDA name has none of the distinctive words the summary uses for the device it names, “Philips device”. Kept off the family tree. Summary page 2.
- K040259: Masimo Set Intellivue Pulse Oximeter Module, Masimo Corp. (2004). Our reading of the summary gave K040259, FDA’s number for Masimo Set Intellivue Pulse Oximeter Module (Masimo Corp.). Its FDA name has none of the distinctive words the summary uses for the device it names, “Philips device”. Kept off the family tree. Summary page 2.

## Most influential descendants
- K050141: The Philips MP20, MP30, MP40, MP50, MP60, MP70 and MP90 Intellivue Patient Monitors (2005), 250 descendants of its own
- K050762: Philips Intellivue Patient Monitor, Models MP20, MP30, MP40, MP50, MP60, MP70 and MP90 (2005), 249 descendants of its own
- K051106: The Philips MP20, MP30, MP40, MP50, MP60, MP70, MP80 and MP90 Intellivue Patient Monitors (2005), 247 descendants of its own
- K052801: Intellivue Patient Monitors with Release C.02, Models MP20, MP30, MP40, MP50, MP60, MP70, MP80 and MP90 (2005), 234 descendants of its own
- K053522: Philips MP40, MP50, MP60, MP70, MP80 and MP90 Intellivue Patient Monitors, Release D.00 (2006), 233 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. The MP20, MP30, MP40 and MP50 are additionally intended for use in transport situations within 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 (tcpO2 /tcpCO 2) is restricted to neonatal patients only.

Source page: https://510kreport.com/device/K042845
Methodology: https://510kreport.com/methodology