ClearanceBrief
510(k) K180685 ยท DQA Oximeter

AS-3XX Series Fingertip Pulse Oximeter

ApplicantXiamen Acurio Instruments Co., Ltd., Xiamen, CN
DecisionSubstantially Equivalent, Nov 29, 2018
ReceivedMar 15, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K180685

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.