ClearanceBrief
510(k) K915073 ยท DQE Catheter, Oximeter, Fiber-Optic

MARQUETTE SV O2 MODULE

ApplicantMarquette Electronics, Inc., Milwaukee WI, US
DecisionSubstantially Equivalent, Dec 29, 1992
ReceivedNov 8, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915073

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.