# K051364: Vpap Adapt

- Pathway: 510(k) (Traditional)
- Applicant: Resmed, Ltd.
- Decided: Aug 16, 2005 after 83 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: 2 generations back to K974417 (1998). 2 ancestors in all.
36 later devices descend from it; 5 cite it directly.
2 of 39 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033276: Vpap Iii ST-a, Resmed, Ltd. (2004) Summary page 1.

## Most influential descendants
- K092186: Vpap TX (2009), 18 descendants of its own
- K063540: Bipap Autosv (2007), 13 descendants of its own
- K102513: S9 Vpap ST with H5I (2011), 11 descendants of its own
- K071560: Provent Nasal Dilator, Model BR2 (2008), 10 descendants of its own
- K113288: Vpap ST-a (2012), 7 descendants of its own

## Indications for use
The VPAP ADAPT is intended to provide non-invasive ventilatory support to treat adult patients with OSA and Respiratory Insufficiency caused by central and/or mixed apneas and periodic breathing.

Source page: https://510kreport.com/device/K051364
Methodology: https://510kreport.com/methodology