# K060105: Vpap Iii ST-a/Kidsta Mask System

- Pathway: 510(k) (Traditional)
- Applicant: Resmed, Ltd.
- Decided: Apr 7, 2006 after 84 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 K961783 (1996). 4 ancestors in all.
53 later devices descend from it; 8 cite it directly.
10 of 58 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.
- K031047: Mirage Vista Mask, Resmed, Ltd. (2003) Summary page 1.

## Most influential descendants
- K063533: Bipap Synchrony (2007), 30 descendants of its own
- K071509: Bipap Synchrony 2 Ventilatory Support System (2007), 28 descendants of its own
- K103167: Stellar 150 (2011), 20 descendants of its own
- K063540: Bipap Autosv (2007), 13 descendants of its own
- K092818: Bipap Avaps Ventilatory Support System (2010), 11 descendants of its own

## Indications for use
The VPAP III ST-A/Kidsta Mask system is intended to provide non-invasive ventilation for pediatric patients aged 7 years or older (>40lbs) with respiratory insufficiency or obstructive sleep apnea (GSA). The device is intended for use in the hospital or home.

Source page: https://510kreport.com/device/K060105
Methodology: https://510kreport.com/methodology