ClearanceBrief
510(k) K252250 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

Vista 300/Vista 300 S; Vista 300 Non-Inv Model A, US (2601064); Vista 300 Invasive Model C, US (2601065); Vista 300 S Non-Inv Model A, US (2602425); Vista 300 S Invasive Model B, US (2602426); Vista 300 S Invasive Model C, US (2602427)

ApplicantShanghai Draeger Medical Instrument Co., Ltd., Shanghai, CN
DecisionSubstantially Equivalent, Apr 10, 2026
ReceivedJul 17, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K252250

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.