ClearanceBrief
510(k) K172890 ยท OLW Index-Generating Electroencephalograph Software

SedLine Sedation Monitor

ApplicantMasimo Corporation, Irvine CA, US
DecisionSubstantially Equivalent, Jan 26, 2018
ReceivedSep 22, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K172890

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.