# K922842: Stylet and Tracheal Lightwand (STL)

- Pathway: 510(k) (Traditional)
- Applicant: Laerdal California, Inc.
- Decided: Dec 18, 1992 after 189 days
- Product code: BSR (Stylet, Tracheal Tube)
- Device class: 1
- Regulation: 21 CFR 868.5790
- 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K954771: Trachlight Stylet & Tracheal Lightwand (Original Application Name: Stylett & Tracheal Lightwand) (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K922842
Methodology: https://510kreport.com/methodology