# K003576: Q-Tel RMS (Rehabilitation Management System), Model 000503

- Pathway: 510(k) (Abbreviated)
- Applicant: Quinton, Inc.
- Decided: Jan 25, 2001 after 66 days
- Product code: DSI (Detector And Alarm, Arrhythmia)
- Device class: 2
- Regulation: 21 CFR 870.1025
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 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
- K041607: Quinton Q-TE; RMS (2004), 4 descendants of its own
- K050778: Telerehad 2004 (2005), 2 descendants of its own
- K212883: ers2 - ergoline Rehabilitation System (2022), 1 descendant of its own
- K250259: TeleRehab Aermos Cardiopulmonary Rehabilitation (2025), 0 descendants of its own
- K173969: Medicalgorithmics Unified Cardiac Rehabilitation System (2018), 0 descendants of its own

## Recalls of this device
- Mar 30, 2009 · Not classified · Z-1757-2010: 28 stress and rehab treadmills manufactured between September 2006 and January 2009 may not have received adequate electrical safety testing prior to being shipped from the factory. If these component

Source page: https://510kreport.com/device/K003576
Methodology: https://510kreport.com/methodology