ClearanceBrief
510(k) K910227 ยท KXO Monitor, Pressure, Intrauterine

MX4043---SERIES, INTRAUTERINE PRESSURE CATHETER

ApplicantMedex, Inc., Hilliard OH, US
DecisionSubstantially Equivalent, Apr 3, 1991
ReceivedJan 18, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910227

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.