ClearanceBrief
510(k) K002939 ยท DQA Oximeter

MODIFICATION TO MASIMO SET RADICAL PULSE OXIMETER WITH SATSHARE AND LNOP SERIES OF SENORS OXIMETER

ApplicantMasimo Corp., Irvine CA, US
DecisionSubstantially Equivalent, Oct 6, 2000
ReceivedSep 21, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K002939

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.