# K051314: Res Traxx Data Center

- Pathway: 510(k) (Traditional)
- Applicant: Resmed, Ltd.
- Decided: Jul 15, 2005 after 56 days
- Product code: BZD (Ventilator, Non-Continuous (Respirator))
- Device class: 2
- Regulation: 21 CFR 868.5905
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K971260 (1997). 7 ancestors in all.
16 later devices descend from it; 1 cites it directly.
0 of 24 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030797: S7 Elite Cpap System with Somnotraxx System; Autoset Spirit Cpap System with Somnotraxx System, Resmed Corp (2004) Summary page 1.

## Most influential descendants
- K053205: Res Traxx Data Center (2006), 15 descendants of its own
- K070746: Restraxx Data Centre, Model R10 (2007), 14 descendants of its own
- K083816: Res Traxx Online, Model: R14 (2009), 13 descendants of its own
- K093684: Easycare Online (2010), 12 descendants of its own
- K123557: Easycare Online (2013), 9 descendants of its own

## Indications for use
The ResTraxx Data Center system is intended to augment the standard follow-up care of adult patients diagnosed with obstructive sleep apnea by providing wireless transmission and display of usage and therapeutic information. It is intended to be used in the home only and with compatible S7 Elite, AutoSet Spirit, AutoSet Respond & S8 Series CPAP Systems, positive airway pressure flow generators.

Source page: https://510kreport.com/device/K051314
Methodology: https://510kreport.com/methodology