ClearanceBrief
510(k) K926450 ยท DQE Catheter, Oximeter, Fiber-Optic

EDSLAB(R) DUAL LUMEN REGION SATUR OXIMETRY CATH

ApplicantBaxter Healthcare Corp, Santa Ana CA, US
DecisionSubstantially Equivalent, Feb 22, 1993
ReceivedDec 24, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K926450

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.