# K001664: Compact Portable Patient Monitor with Wireless Alan, Model Alilent M3000A/M3046A Option J120

- Pathway: 510(k) (Special)
- Applicant: Agilent Technologies, Inc.
- Decided: Jun 30, 2000 after 30 days
- Product code: MHX (Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms))
- 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.
405 later devices descend from it; 5 cite it directly.
0 of 406 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
- 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
- K040259: Masimo Set Intellivue Pulse Oximeter Module (2004), 312 descendants of its own
- K040357: M3290A Intellivue Information Center Software Release F.O and the M4840A Telemetry Monitoring System II (2004), 260 descendants of its own

Source page: https://510kreport.com/device/K001664
Methodology: https://510kreport.com/methodology