# K011339: Quest Exercise Stress System, Model Configuration 14

- Pathway: 510(k) (Traditional)
- Applicant: Spacelabs Burdick, Inc.
- Decided: Aug 20, 2001 after 110 days
- Product code: DSI (Detector And Alarm, Arrhythmia)
- 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.
6 later devices descend from it; 2 cite it directly.
0 of 7 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
- K024283: Cardiodirect, Models 12M, 12I, 12S (2003), 4 descendants of its own
- K093211: Carecenter MD (2010), 1 descendant of its own
- K123217: Cardeascreen (2013), 0 descendants of its own
- K082380: Vicardio 12B (2008), 0 descendants of its own
- K062469: Voyager 12 (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K011339
Methodology: https://510kreport.com/methodology