ClearanceBrief
510(k) K172141 ยท DQA Oximeter

Pulse Oximeter

ApplicantShanghai Berry Electronic Tech Co., Ltd., Shanghai, CN
DecisionSubstantially Equivalent, Apr 4, 2018
ReceivedJul 17, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K172141

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.