# K053205: Res Traxx Data Center

- Pathway: 510(k) (Traditional)
- Applicant: Resmed, Ltd.
- Decided: Feb 3, 2006 after 79 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: 4 generations back to K971260 (1997). 8 ancestors in all.
15 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)
- K051314: Res Traxx Data Center, Resmed, Ltd. (2005) Summary page 1.

## Most influential descendants
- 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
- K132371: Easycare Online (2013), 8 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, VPAP III & S8 Series CPAP Systems, positive airway pressure flow generators.

Source page: https://510kreport.com/device/K053205
Methodology: https://510kreport.com/methodology