# K223398: Gastric Alimetry System

- Pathway: 510(k) (Traditional)
- Applicant: Alimetry, Ltd.
- Decided: Apr 27, 2023 after 170 days
- Product code: MYE (System, Electrogastrography (Egg))
- Device class: 2
- Regulation: 21 CFR 876.1735
- 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 DEN990005 (1999). 3 ancestors in all.
4 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K213924: Gastric Alimetry System, Alimetry, Ltd. (2022) Summary page 4.

## Most influential descendants
- K232925: Gastric Alimetry System (2023), 3 descendants of its own
- K240946: Gastric Alimetry (2024), 2 descendants of its own
- K252504: Gastric Alimetry (2025), 1 descendant of its own
- K262292: Gastric Alimetry (2026), 0 descendants of its own

## Indications for use
The Gastric Alimetry System is intended to record, store, view and process gastric myoelectrical activity as an aid in the diagnosis of various gastric disorders.

Source page: https://510kreport.com/device/K223398
Methodology: https://510kreport.com/methodology