ClearanceBrief
510(k) K211143 ยท DQA Oximeter

Pulse Oximeter

ApplicantShenzhen Brav Electronic Technologies Co., Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Jul 17, 2023
ReceivedApr 16, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K211143

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.