# K000635: Modification to HP M2376A Device Link System

- Pathway: 510(k) (Special)
- Applicant: Agilent Technologies, Inc.
- Decided: Mar 20, 2000 after 24 days
- Product code: MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms))
- Device class: 2
- Regulation: 21 CFR 870.2300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
14 later devices descend from it; 1 cites it directly.
0 of 15 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
- K013019: Datacaptor (2001), 13 descendants of its own
- K020197: Modification to Datacaptor (2002), 12 descendants of its own
- K032142: Datacaptor (2003), 11 descendants of its own
- K040969: Poise Dataengine (2004), 6 descendants of its own
- K101571: Xper Information Management and Flex Cardio Physiomonitoring Systems (2010), 5 descendants of its own

Source page: https://510kreport.com/device/K000635
Methodology: https://510kreport.com/methodology