# K003038: Agilent Component Monitoring System, Agilent V24/26, Agilent Bis Module, Model M1175A/76A/77A,Rev.L,M1205A,Rev.L,M1034A

- Pathway: 510(k) (Traditional)
- Applicant: Agilent Technologies Deutschland GmbH
- Decided: Dec 15, 2000 after 77 days
- Product code: OLW (Index-Generating Electroencephalograph Software)
- Device class: 2
- Regulation: 21 CFR 882.1400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
409 later devices descend from it; 2 cite it directly.
0 of 410 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
- K021778: Philips Component Compact Monitor, Release a.04, Model #M1275B (2002), 407 descendants of its own
- K023871: M3046A (M2/M3/M4) Compact Portable Patient Monitor and MP60 & MP70 Intellivue Patient Monitor with Portal Technology (2002), 406 descendants of its own
- K030038: Philips MP60, MP70 and MP90 Intellivue Patient Monitors with Portal Technology and M3185 Opt C41 Wireless Bedside Adaptr (2003), 404 descendants of its own
- K031481: The Philips Intellivue MP60, MP70, and MP90 Patient Monitors, Release a.20 (2003), 376 descendants of its own
- K032858: The Philips Intellivue MP40, MP50, MP60, MP70,and MP90 Patient Monitors, Release B.O. (2003), 375 descendants of its own

Source page: https://510kreport.com/device/K003038
Methodology: https://510kreport.com/methodology