# K212407: Gastric Lightguide (GLG)

- Pathway: 510(k) (Traditional)
- Applicant: Naser Dib Gabinet Lekarksi Nasmed
- Decided: Jul 26, 2022 after 357 days
- Product code: KNT (Tubes, Gastrointestinal (And Accessories))
- Device class: 2
- Regulation: 21 CFR 876.5980
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K002838 (2001). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130483: Boehringer Gastric Sizing Tube, Boehringer Laboratories, LLC (2013) Summary page 4.

## Indications for use
Use in gastric and bariatric surgical procedures for the application of suction, stomach decompression and drainage of gastric fluids and irrigation. Patient Population: For use in Adults only

Source page: https://510kreport.com/device/K212407
Methodology: https://510kreport.com/methodology