ClearanceBrief
510(k) K111451 ยท HCG Device, Neurovascular Embolization

MICROPLEX COIL SYSTEM-VECTOR MODEL 030606XXX-V, 030610XXX-V, 30615XXX-V, 061020XXX-V, 061030XXX-V, 101530XXX-V, 101540XX

ApplicantMicroVention, Inc., Tistin CA, US
DecisionSubstantially Equivalent, Sep 20, 2011
ReceivedMay 25, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K111451

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.