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GE HealthCare Submits Modeling Software for FDA Approval

Posted on May 29, 2026
By Google News
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GE HealthCare Submits Modeling Software for FDA Approval

May 29, 2026 — GE HealthCare recently announced that its MIM KineticID modeling software1 is now 510(k) pending with the U.S. Food and Drug Administration. MIM KineticID is engineered to enable dynamic PET workflows and kinetic modeling to deliver a clear, data-driven view of how radiotracers behave across the body over time — helping support more confident clinical and research decisions.