FDA cleared the Gastric Alimetry from Alimetry , Ltd. on Sep 4, 2026 under K262292, a traditional 510(k). The device falls under product code MYE, System, Electrogastrography (Egg), regulated at 21 CFR 876.1735 as a Class 2 device. The review panel was Gastroenterology, Urology.
FDA logged the submission as received on Jul 7, 2026. The decision came 59 days later, inside the 90 FDA-day goal for a 510(k).
Alimetry , Ltd. has one other decision in the tracker over the last 12 months: K252504 (Gastric Alimetry).