# K151901: AirView

- Pathway: 510(k) (Traditional)
- Applicant: Resmed, Ltd.
- Decided: Nov 5, 2015 after 118 days
- Product code: CBK (Ventilator, Continuous, Facility Use)
- 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: 10 generations back to K971260 (1997). 51 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 53 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K132371: Easycare Online, Resmed, Ltd. (2013) Summary page 5.
- K140054: Rescan, Resmed, Ltd. (2014) Summary page 5.

## Most influential descendants
- K242485: EveryWare (2025), 0 descendants of its own

## Indications for use
AirView is a web based solution for healthcare specialists intended to: - assist in the diagnosis of sleep disordered breathing in adult patients through analysis of data recorded by an AirView compatible home sleep device. - transfer and display machine and therapeutic information that has been transmitted remotely from the patient's therapy device. It is intended to support the standard follow-up care of patients that have been prescribed a compatible ResMed therapy device. AirView also provides remote settings capabilities for non-life support devices only.

Source page: https://510kreport.com/device/K151901
Methodology: https://510kreport.com/methodology