ClearanceBrief
510(k) K233963 ยท DQA Oximeter

Aulisa Oximeter Module (2nd Gen.) (GA-OM0007, GA-OM0008)

ApplicantTaiwan Aulisa Medical Devices Technologies, Inc., Taipei City, TW
DecisionSubstantially Equivalent, Feb 25, 2025
ReceivedDec 15, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233963

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.