# K262292: Gastric Alimetry

- Pathway: 510(k) (Traditional)
- Applicant: Alimetry, Ltd.
- Decided: Sep 4, 2026 after 59 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: 7 generations back to DEN990005 (1999). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K252504: Gastric Alimetry, Alimetry, Ltd. (2025) Summary page 5.

## 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. The Gastric Alimetry System is indicated for patients 12 years and older.

Source page: https://510kreport.com/device/K262292
Methodology: https://510kreport.com/methodology