# K812648: Ehtox Gastric Lavage Kit #2050 & #2070

- Pathway: 510(k) (Traditional)
- Applicant: Ethox Corp.
- Decided: Sep 29, 1981 after 12 days
- Product code: KNT (Tubes, Gastrointestinal (And Accessories))
- Device class: 2
- Regulation: 21 CFR 876.5980
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Recalls of this device
- Mar 25, 2011 · Not classified · Z-0271-2012: Ethox Tum-E-Vac Gastric Lavage Kit #2075, Lot Number 031123255 was labeled with expiration date symbol and date of 2010/10 on the unit product label. The carton was labeled with a manufacturing date s

Source page: https://510kreport.com/device/K812648
Methodology: https://510kreport.com/methodology