# K092186: Vpap TX

- Pathway: 510(k) (Traditional)
- Applicant: Resmed, Ltd.
- Decided: Dec 22, 2009 after 154 days
- Product code: MNS (Ventilator, Continuous, Non-Life-Supporting)
- Device class: 2
- Regulation: 21 CFR 868.5895
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K971260 (1997). 17 ancestors in all.
18 later devices descend from it; 5 cite it directly.
0 of 36 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051364: Vpap Adapt, Resmed, Ltd. (2005) Summary page 1.
- K080131: Vpap ST, Resmed, Ltd. (2008) Summary page 1.
- K033276: Vpap Iii ST-a, Resmed, Ltd. (2004) Summary page 1.
- K952429: Res Care Auto Set Clinical, Portable System, Portable 2 System, Rescare, Ltd. (1996) Summary page 1.

## Most influential descendants
- K102513: S9 Vpap ST with H5I (2011), 11 descendants of its own
- K113288: Vpap ST-a (2012), 7 descendants of its own
- K102586: S9 Vpap Adapt with H5I (2011), 6 descendants of its own
- K113801: Vpap Adapt (2012), 5 descendants of its own
- K153061: Juno VPAP ST-A (2016), 3 descendants of its own

## Indications for use
The VPAP Tx is indicated for the treatment of patients weighing more than 66 lb (> 30 kg) with obstructive sleep apnea (OSA), respiratory insufficiency, central or mixed apneas, or periodic breathing. The VPAP Tx is intended to be used in a clinical environment.

Source page: https://510kreport.com/device/K092186
Methodology: https://510kreport.com/methodology