# K000854: Viridia Information Center Software for M3150A and M3153A, Viridia Telemetry System Transmitter

- Pathway: 510(k) (Special)
- Applicant: Agilent Technologies, Inc.
- Decided: Apr 10, 2000 after 25 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.
10 later devices descend from it; 3 cite it directly.
0 of 11 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
- K081983: M3290A Intellivue Information Center Software, Release 1.00 (2008), 8 descendants of its own
- K102495: M3290B Intellivue Information Center Software, Release a.0 (2010), 7 descendants of its own
- K143057: M3290B Philips IntelliVue Information Center iX (2014), 4 descendants of its own
- K153702: M3290B Philips IntelliVue Information Center iX (2016), 3 descendants of its own
- K163584: M3290B Philips IntelliVue Information Center iX (2017), 2 descendants of its own

Source page: https://510kreport.com/device/K000854
Methodology: https://510kreport.com/methodology