# K945626: Quinton Model 710 Stress Electrocardiograph

- Pathway: 510(k) (Traditional)
- Applicant: Quinton, Inc.
- Decided: Jun 28, 1995 after 224 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.
32 later devices descend from it; 2 cite it directly.
0 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K964784: Synergy Cardiology Information System (00431) (1997), 29 descendants of its own
- K032038: Pyramis Ecg Management System Model Numbers, 92600 and 92601 (2003), 20 descendants of its own
- K050858: Ascentia Heartstation Ecg Management System (2005), 13 descendants of its own
- K061905: Horizon Cardiology Ecg-Mckesson's Ecg Management System, Model 1.0 (2006), 8 descendants of its own
- K113515: Horizon Cardiology Ecg Management (2012), 7 descendants of its own

Source page: https://510kreport.com/device/K945626
Methodology: https://510kreport.com/methodology