ClearanceBrief
510(k) K142888 ยท DQA Oximeter

Fingertip Pulse Oximeter

ApplicantBeijing Choice Electronic Technololgy Co., Ltd., Beijing, CN
DecisionSubstantially Equivalent, Feb 20, 2015
ReceivedOct 2, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K142888

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.