# K844296: Tracheal Tube, Reinforced, Cuffed

- Pathway: 510(k) (Traditional)
- Applicant: Sheridan Catheter Corp.
- Decided: Dec 4, 1984 after 28 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.
3 later devices descend from it; 3 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K192324: Sheridan Spiral-Flex Endotracheal Tubes (2019), 0 descendants of its own
- K955495: Rusch Reinforced Trachael Tube Cuffed, Sterile (1996), 0 descendants of its own
- K954585: Rusch Pediatric Reinforced Traheal (or Endotracheal) Tube - Uncuffed, Sterile (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K844296
Methodology: https://510kreport.com/methodology