ClearanceBrief
510(k) K250837 ยท DQA Oximeter

Pulse Oximeter

ApplicantShanghai Berry Electronic Tech Co., Ltd., Shanghai, CN
DecisionSubstantially Equivalent, Sep 25, 2025
ReceivedMar 20, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K250837

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.