# K951696: Endotracheal Tube

- Pathway: 510(k) (Traditional)
- Applicant: Unomedical Sdn Bhd
- Decided: May 22, 1995 after 40 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.
1 of 2 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K091591: Flexicare Medical Endotracheal Tubes (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K951696
Methodology: https://510kreport.com/methodology