# K002758: Agilent Component Monitoring System, Agilent Cardiac Output Module, Agilent Invasive Pressure Module, Model M1175A/76A

- Pathway: 510(k) (Traditional)
- Applicant: Agilent Technologies Deutschland GmbH
- Decided: Feb 22, 2001 after 170 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
No predicates in its family tree.
158 later devices descend from it; 2 cite it directly.
0 of 159 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K033444: Philips Medical Systems, M3012A- Hemodynamic Extension to the Multi-Measurement Server (2003), 156 descendants of its own
- K071426: MP2, X2, MP5, MP20, MP30, MP40, MP50, MP60, MP70, MP80, and MP90  Intellivue Patient Monitors (2007), 151 descendants of its own
- K082633: Intellivue Patient Monitor, Intellivue XDS, Models MP2, MP5, MP20, MP30, MP40, MP50, MP60, MP70, MP80, MP90 (2008), 127 descendants of its own
- K083517: Intellivue Patient Monitor, Models MP2, MP5, MP20, MP30, MP40, MP50, MO60, MP7-, MP80, and MP90 (2009), 125 descendants of its own
- K091927: Intellivue Patient Monitors ,Models MP40, MP50, MP60, MP70, MP80, MP90 (2009), 124 descendants of its own

Source page: https://510kreport.com/device/K002758
Methodology: https://510kreport.com/methodology