510(k) Report

510(k) · Cleared

Cleared

Gastric Alimetry

K252504510(k) TraditionalCleared Dec 5, 2025119-day reviewClass II21 CFR 876.1735

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Alimetry, Ltd. · MYE System, Electrogastrography (Egg)

Cleared on Dec 5, 2025 as substantially equivalent to K240946 (Alimetry, Ltd., 2024) after a 119-day review. Its family tree reaches back 6 generations to 1999. 1 later device descends from it.

Decided
Dec 5, 2025
Review
119 days
Class
Class II
Product code
MYE
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to DEN990005 (1999). 1 later device descends from it, 1 citing it directly.

  1. Root · 6 generations backDEN990005 The 3PM Egg Machine3pm Co., Inc. · 1999
  2. 5 generations backK014269 Polygram Net Electrogastrography Application Software, Model…Medtronic Functional Diagnostics A/S · 2002
  3. 4 generations backK213924 Gastric Alimetry SystemAlimetry, Ltd. · 2022
  4. 3 generations backK223398 Gastric Alimetry SystemAlimetry, Ltd. · 2023
  5. 2 generations backK232925 Gastric Alimetry SystemAlimetry, Ltd. · 2023
  6. 1 generation backK240946 Gastric AlimetryAlimetry, Ltd. · 2024
  7. This deviceK252504 Gastric AlimetryAlimetry, Ltd. · 2025
  8. Descendant · cites it directly · 0 of its ownK262292 Gastric AlimetryAlimetry, Ltd. · 2026

Most influential descendants

Showing 1 of 1 · See all
  • K262292Gastric AlimetryAlimetry, Ltd. · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6DEN990005The 3PM Egg Machine3pm Co., Inc.1999—
−5K014269Polygram Net Electrogastrography Application Software, Model 9043S0151…Medtronic Functional Diagnostics A/S2002—
−4K213924Gastric Alimetry SystemAlimetry, Ltd.2022—
−3K223398Gastric Alimetry SystemAlimetry, Ltd.2023—
−2K232925Gastric Alimetry SystemAlimetry, Ltd.2023—
−1K240946Gastric AlimetryAlimetry, Ltd.2024—
0 (this device)K252504Gastric AlimetryAlimetry, Ltd.2025—
+1K262292Gastric AlimetryAlimetry, Ltd.2026—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K252504, 1999–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in MYE? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new MYE device

  1. #1 K262292 Gastric Alimetryscore 13.8 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K240946Gastric Alimetry
Summary page 5
…ystem Classification Name: Electrogastrography system, 21 CFR 876.1735 Regulatory Class: Class II Product Code: MYE Predicate Devices Trade Name: Gastric Alimetry (K240946) (primary predicate) Manufacturer: Alimetry Ltd. Device Description The Gastric Alimetry System is an electrogastrography (EG…
Alimetry, Ltd.2024—

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K262292Gastric AlimetryAlimetry, Ltd.20260

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 26 years and passes through 3 companies; a new generation was cleared every 1.4 years on median.
  • None of the 6 ancestors has a recall.
  • Of its descendants, K262292 (Alimetry, Ltd., 2026) has gone furthest, with 0 descendants of its own.

How does its category compare?

All MYE devices

MYE System, Electrogastrography (Egg): FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.

FDA decisions per year · MYE

1in 2025

2022: 22023: 22024: 12025: 12026 (partial year): 1
2007high 2 (2022) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MYE

Too few MYE 510(k)s in any year since 2007 to give a median.

Recalls per year · MYE

No recall names MYE since 2007.

Adverse event reports per year · MYE

No MAUDE report names MYE since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20222—00
20232—00
20241—00
20251—00
20261—0—

What is it indicated for?

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

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K252504: Gastric Alimetry.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K252504

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026