ClearanceBrief
510(k) K202776 ยท DQA Oximeter

Fingertip pulse oximeter

ApplicantShenzhen Lepu Intelligent Medical Equipment Co., Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Mar 1, 2021
ReceivedSep 21, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K202776

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.