ClearanceBrief
510(k) K933723 ยท LKF Cannula, Manipulator/Injector, Uterine

CONCEPTUS UTERINE CATHETER

ApplicantConceptus, Inc., San Carlos CA, US
DecisionSubstantially Equivalent, Dec 27, 1994
ReceivedAug 2, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K933723

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.