ClearanceBrief
510(k) K191430 ยท DQA Oximeter

Pulse Oximeter

ApplicantShenzhen Yimi Life-Technology Co., Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Oct 18, 2019
ReceivedMay 29, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K191430

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.