# K030792: Bard Endotracheal Tube, Cuffed

- Pathway: 510(k) (Traditional)
- Applicant: C.R. Bard, Inc.
- Decided: Nov 14, 2003 after 247 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Mallinckrodt Hi-Lo/Intermediate Hi-Lo Tracheal Tube, Cuffed: named in the summary without a submission number

## Indications for use
The Bard Endotracheal Tube, Cuffed is indicated for airway management by oralhasal intubation of the trachea for anesthesia

Source page: https://510kreport.com/device/K030792
Methodology: https://510kreport.com/methodology