# K002459: Pagewriter 10/10I, Model M2662A Handheld Electrocardiograph

- Pathway: 510(k) (Traditional)
- Applicant: Agilent Technologies, Inc.
- Decided: Nov 8, 2000 after 90 days
- Product code: DPS (Electrocardiograph)
- Device class: 2
- Regulation: 21 CFR 870.2340
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 1 cites it directly.
0 of 10 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
- K013367: Cardiocollect Portable Electrocardiograph (2001), 8 descendants of its own
- K024283: Cardiodirect, Models 12M, 12I, 12S (2003), 4 descendants of its own
- K053083: Datrix Cardio Wifi Electrocardiograph (2005), 2 descendants of its own
- K103427: Mobileecg System (2011), 1 descendant of its own
- K093211: Carecenter MD (2010), 1 descendant of its own

Source page: https://510kreport.com/device/K002459
Methodology: https://510kreport.com/methodology