ClearanceBrief
510(k) K860101 ยท KXO Monitor, Pressure, Intrauterine

MX4040 INTRAUTERINE PRESSURE MONITORING KIT

ApplicantMedex, Inc., Hilliard OH, US
DecisionSubstantially Equivalent, Apr 14, 1986
ReceivedJan 10, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860101

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.