ClearanceBrief
510(k) K240305 ยท DQA Oximeter

ANNE Limb

ApplicantSibel Health, Inc., Chicago IL, US
DecisionSubstantially Equivalent, May 28, 2024
ReceivedFeb 2, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K240305

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.