ClearanceBrief
510(k) K092980 ยท LKF Cannula, Manipulator/Injector, Uterine

PANPAC UTERINE MANIPULATOR INJECTOR, MODEL UMI 4.5

ApplicantPanpac Medical Corporation, Shi-Chih City, Taipei Hsien, TW
DecisionSubstantially Equivalent, Mar 11, 2010
ReceivedSep 28, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092980

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.