ClearanceBrief
510(k) K160582 ยท DQA Oximeter

WiCap

ApplicantAthena Gtx, Johnson IA, US
DecisionSubstantially Equivalent, Sep 2, 2016
ReceivedMar 1, 2016
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K160582

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.