ClearanceBrief
510(k) K120107 ยท HHE Cup, Menstrual

SCKOONCUP

ApplicantSckoon, Inc., Miami Beach FL, US
DecisionSubstantially Equivalent, Sep 18, 2012
ReceivedJan 13, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K120107

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.