ClearanceBrief
510(k) K862873 ยท KXO Monitor, Pressure, Intrauterine

IUC - INTRAUTERINE CATHETER

ApplicantUtah Medical Products, Inc., Midvale UT, US
DecisionSubstantially Equivalent, Feb 26, 1987
ReceivedJul 30, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862873

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.