ClearanceBrief
510(k) K012935 ยท MFD Cannula, Intrauterine Insemination

THECURVE, ITEM 507

ApplicantSelect Medical Systems, Inc., Williston VT, US
DecisionSubstantially Equivalent, Oct 11, 2001
ReceivedAug 31, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K012935

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.