# K111406: Bever Reinforced Endotracheal Tube with Cuff (Oral/Nasal), Bever Reinforced Endotracheal Tube Without Cuff (Oral/Nasal)

- Pathway: 510(k) (Traditional)
- Applicant: Hangzhou Bever Medical Devices Co., Ltd.
- Decided: Jul 19, 2012 after 427 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: 6 generations back to K903730 (1990). 19 ancestors in all.
1 later device descends from it; 1 cites it directly.
4 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073383: Well Lead Reinforced Endotracheal Tube, Well Lead Medical Instruments (2008) Summary page 1.
- K032112: P0RTEX Reinforced Tracheal Tube (Cuffed and Uncuffed), Portex, Ltd. (2004) Summary page 1.

## Most influential descendants
- K170234: Endotracheal tube; Reinforced Endotracheal tube (2018), 0 descendants of its own

## Indications for use
The BEVERm Reinforced Endotracheal Tube is indicated for airway management by oral or nasal intubation of the trachea during anesthesia. The product may be used where the patient's neck is likely to be moved or flexed or the patient is in the prone position so that a non-reinforced tracheal tube might become kinked.

Source page: https://510kreport.com/device/K111406
Methodology: https://510kreport.com/methodology