Product code MYE— Gastroenterology, Urology

Gastric Alimetry

Classification name
System, Electrogastrography (Egg)
Device class
Class 2
Regulation
21 CFR 876.1735
Advisory panel
Gastroenterology, Urology
Total cleared
9
First cleared
Most recent

Market context for product code MYE

FDA has cleared 9 devices under product code MYE between 1999 and 2026, filed by 4 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

Top applicants under product code MYE

Recent clearances under product code MYE

Data sourced from openFDA. This site is unofficial and independent of the FDA.