ClearanceBrief
510(k) K223399 ยท DQA Oximeter

AViTA Pulse Oximeter

ApplicantAvita Corporation, New Taipei City, TW
DecisionSubstantially Equivalent, May 20, 2024
ReceivedNov 9, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K223399

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.