ClearanceBrief
510(k) K180174 ยท DQA Oximeter

Belun Ring

ApplicantBelun Technology Company Limited, Sha Tin, HK
DecisionSubstantially Equivalent, May 29, 2018
ReceivedJan 22, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K180174

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.