# K082174: Y-Adapter

- Pathway: 510(k) (Traditional)
- Applicant: Asthmatx, Inc.
- Decided: Oct 20, 2008 after 80 days
- Product code: KTI (Bronchoscope Accessory)
- Device class: 2
- Regulation: 21 CFR 874.4680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K931154 (1993). 21 ancestors in all.
No later device cites it as a predicate yet.
2 of 22 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061313: Evis Exera 180 System, Olympus Medical Systems Corporation (2006) Summary page 1.

## Indications for use
For use in the delivery of fluids via the instrument channel of a bronchoscope. For single use only.

Source page: https://510kreport.com/device/K082174
Methodology: https://510kreport.com/methodology