# K142467: IntelAir Nasal Airway Support System

- Pathway: 510(k) (Special)
- Applicant: Abeon Medical Corporation
- Decided: Nov 24, 2014 after 82 days
- Product code: CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase)
- Device class: 2
- Regulation: 21 CFR 868.1400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K131506 (2014). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131506: Airway Support System / Airport, Abeon Medical Corporation (2014) Summary page 4.

## Indications for use
The device is indicated for use in patients requiring supplemental oxygenation, patients requiring capnographic monitoring, and patients requiring non-definitive airway support. To be used in one or any combination of the preceding circumstances.

Source page: https://510kreport.com/device/K142467
Methodology: https://510kreport.com/methodology