# K083816: Res Traxx Online, Model: R14

- Pathway: 510(k) (Traditional)
- Applicant: Resmed, Ltd.
- Decided: Mar 20, 2009 after 88 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: 6 generations back to K971260 (1997). 10 ancestors in all.
13 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)
- K070746: Restraxx Data Centre, Model R10, Resmed, Ltd. (2007) Summary page 1.

## Most influential descendants
- 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
- K152356: Sapphire (2016), 4 descendants of its own
- K181053: Care Orchestrator (2019), 1 descendant of its own

## Indications for use
ResTraxx Online is intended to augment the standard follow-up care of patients diagnosed with obstructive sleep apnea by displaying usage and therapeutic information that has been wirelessly transmitted from the patient's flow generator located in the home to the care giver. ResTraxx Online also provides remote settings capabilities. It is intended to be used in the home only and with compatible S7 Elite, AutoSet Spirit, AutoSet Respond, S8 Series CPAP Systems, VPAP III, VPAP III ST, VPAP Malibu, VPAP Auto, VPAP Auto 25, VPAP S and VPAP ST variants positive airway pressure flow generators.

Source page: https://510kreport.com/device/K083816
Methodology: https://510kreport.com/methodology