# FEG: Tube, Double Lumen For Intestinal Decompression And/Or Intubation

- Device class: 2; regulation: 21 CFR 876.5980; FDA's rule: 510(k) required
- FDA decisions: 13
- Recalls: 13 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 1988: 1
- 1990: 1
- 1992: 1
- 1995: 2
- 1996: 1
- 1997: 1
- 2004: 1
- 2006: 1
- 2013: 1
- 2017: 1

## Most-cited predicates
- K960176: Davol Nasogastric Sump Tube W/Prevent Filter (1996), cited by 3
- K040388: Next Generation Salem Sump (2004), cited by 2
- K935781: Argyle Salem Sump Tube Anti-Reflux Valve Insertion Tray (1995), cited by 2
- K921104: Lopez Valve with NG Sump Tube (1992), cited by 1
- K900035: Wilson-Cook Colon Decompression Set (1990), cited by 1
- K971354: Knott NG Tube (1997), cited by 1

Source page: https://510kreport.com/product-code/FEG
Data by year (CSV): https://510kreport.com/product-code/FEG.csv