ClearanceBrief
510(k) K030640 ยท DQA Oximeter

SIEMENS MICRO2+ WITH VAI SOFTWARE

ApplicantSiemens Medical Solutions USA, Inc., Danvers MA, US
DecisionSubstantially Equivalent, Jun 3, 2003
ReceivedFeb 28, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K030640

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.