ClearanceBrief
510(k) K031515 ยท DQA Oximeter

SPIROPRO SPO2

ApplicantViasys Healthcare GmbH, Yorba Linda CA, US
DecisionSubstantially Equivalent, Nov 14, 2003
ReceivedMay 14, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031515

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.