FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇿 New Zealand

Gastric Alimetry

K Number: K252504 · Decision Dec 5, 2025
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
7
Applicant Total
5
Review Days
119

Basic Information

Device Name
Gastric Alimetry
K Number
K252504
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1735
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alimetry , Ltd.
Date Received
August 8, 2025
Decision Date
December 5, 2025
Product Code
MYE
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MYE System, Electrogastrography (Egg)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MYE), ordered by most recent decision date.

View all

Other Clearances by Alimetry , Ltd.

K Number Device Name
K240946 Gastric Alimetry
K232925 Gastric Alimetry System
K223398 Gastric Alimetry System
K213924 Gastric Alimetry System