# K954771: Trachlight Stylet & Tracheal Lightwand (Original Application Name: Stylett & Tracheal Lightwand)

- Pathway: 510(k) (Traditional)
- Applicant: Laerdal Medical Corp.
- Decided: May 9, 1996 after 205 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
Longest line of descent: 1 generation back to K922842 (1992). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K922842: Stylet and Tracheal Lightwand (STL), Laerdal California, Inc. (1992) Summary page 2.
- (no number) Fiberoptic Medical Products, Inc. Imagica Fiberoptic Lighted Stylet: named in the summary without a submission number
- (no number) Aaron Medical Industries, AARON Pediatric Surch-Lite: named in the summary without a submission number

## Indications for use
The Trachlight is designed to facilitate the placement of endotracheal tubes of various sizes and lengths for both orotracheal and nasotracheal intubations.

Source page: https://510kreport.com/device/K954771
Methodology: https://510kreport.com/methodology