# K131506: Airway Support System / Airport

- Pathway: 510(k) (Traditional)
- Applicant: Abeon Medical Corporation
- Decided: Mar 6, 2014 after 286 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K142467: IntelAir Nasal Airway Support System (2014), 0 descendants of its own

## Indications for use
*theAir~ort is indicated for use in patients requiring supplemenital oiygenatidn, patint requiring capifographic monitoring, and patients requiring non-definitive airway support To be used in one or any combiniation of the preceding circumstances.

Source page: https://510kreport.com/device/K131506
Methodology: https://510kreport.com/methodology