# K192120: Venner PneuX™ ETT (Endotracheal Tube)  6 mm,  Venner PneuX™ ETT (Endotracheal Tube)  7 mm,  Venner PneuX™ ETT (Endotracheal Tube)  8 mm,  Venner PneuX™ ETT (Endotracheal Tube)  9 mm

- Pathway: 510(k) (Traditional)
- Applicant: Venner Medical (Singapore) Pte, Ltd.
- Decided: Feb 14, 2020 after 192 days
- Product code: BTR (Tube, Tracheal (W/Wo Connector))
- Device class: 2
- Regulation: 21 CFR 868.5730
- 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 K093135 (2010). 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)
- K093135: Venner Pneux P.Y. (TM) Tracheostomy Tube and Endo Tracheal Tube, Venner Medical (Singapore) Pte, Ltd. (2010) Summary page 5.

## Indications for use
The Venner PneuX™ ETT (Endotracheal Tube) is intended to be used for patients undergoing tracheal intubation during routine anesthesia or over extended periods (not more than 30 days) and for the evacuation or drainage of secretion from the subglottic space.

Source page: https://510kreport.com/device/K192120
Methodology: https://510kreport.com/methodology