ClearanceBrief
510(k) K061679 ยท LKF Cannula, Manipulator/Injector, Uterine

WALLACE ARTIFICIAL INSEMINATION CATHETER

ApplicantIrvine Scientific Sales Co., Inc., Santa Ana CA, US
DecisionSubstantially Equivalent, Oct 13, 2006
ReceivedJun 15, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061679

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.