ClearanceBrief
510(k) K910742 ยท KXO Monitor, Pressure, Intrauterine

MEDI-TRACE DISPOSABLE INTRAUTERINE CATHETER

ApplicantGraphic Controls Corp., Buffalo NY, US
DecisionSubstantially Equivalent, Jan 14, 1992
ReceivedFeb 21, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910742

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.