ClearanceBrief
510(k) K152390 ยท DQA Oximeter

Medke Oximetry Finger Sensor

ApplicantShenzhen Medke Technology Co., Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Aug 18, 2016
ReceivedAug 24, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K152390

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.