# K090360: Philips M3001A Multi Measurement Server

- Pathway: 510(k) (Special)
- Applicant: Philips Medizin Systeme Boblingen GmbH
- Decided: May 4, 2009 after 81 days
- Product code: DQA (Oximeter)
- Device class: 2
- Regulation: 21 CFR 870.2700
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K941811 (1994). 54 ancestors in all.
84 later devices descend from it; 2 cite it directly.
0 of 139 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030973: Picosat II SPO2 Pulse Oximetry Module, Philips Medical Systems (2003) Summary page 1.
- K033715: Picosat II SP02 Pulse Oximetry Module and M3001A Multi-Measurement Server, Philips Medical Systems, Inc. (2004) Summary page 1.
- K060576: Nellcor Oximax N-600X Pulse Oximeter, Nellcor Puritan Bennett, Inc. (2006) Summary page 1.

## Most influential descendants
- K120366: Intellivue Patient Monitor (2012), 46 descendants of its own
- K122439: Intellivue Patient Monitor (2012), 41 descendants of its own
- K131872: Intellivue Patient Monitor MX500, Intellivue Patient Monitor MX550 (2013), 37 descendants of its own
- K130849: Intellivue Patient Monitor MX400; Intellivue Patient Monitor MX450 (2013), 37 descendants of its own
- K101600: Intellivue CL SP02 Pod Model 865215, Intellivue CL NBP Pod Model 865216, Intellivue Patient Monitors MP5, MP2, X2 Model (2010), 37 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 adult, pediatric and neonatal patients in a hospital environment and during transport inside and outside of hospital environment.

Source page: https://510kreport.com/device/K090360
Methodology: https://510kreport.com/methodology