ClearanceBrief
510(k) K250233 ยท DXH Transmitters And Receivers, Electrocardiograph, Telephone

PreemptiveAI Clinical SDK

ApplicantMeasure Labs, Inc. (Dba Preemptiveai, Inc.), Seattle WA, US
DecisionSubstantially Equivalent, Feb 13, 2026
ReceivedJan 27, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K250233

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.