ClearanceBrief
510(k) K071024 ยท DQA Oximeter

MODIFICATION TO: RAINBOW ADHESIVE CO-OXIMETRY SENSORS

ApplicantMasimo Corporation, Irvine CA, US
DecisionSubstantially Equivalent, Jun 29, 2007
ReceivedApr 11, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K071024

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.