# K093135: Venner Pneux P.Y. (TM) Tracheostomy Tube and Endo Tracheal Tube

- Pathway: 510(k) (Traditional)
- Applicant: Venner Medical (Singapore) Pte, Ltd.
- Decided: Apr 2, 2010 after 179 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
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
- 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 (2020), 0 descendants of its own

## Indications for use
The Venner PneuxP.Y.™ EndoTracheal Tube (ETT) is an endotracheal tube intended to be used for patients undergoing tracheal tube intubation during extended periods (not more than 30 deays) and for evacuation or drainage of secretion from the subglottice space. It is also compatible with tracheal intubation during routine anesthesia.

Source page: https://510kreport.com/device/K093135
Methodology: https://510kreport.com/methodology