ClearanceBrief
510(k) K082739 ยท HCG Device, Neurovascular Embolization

MICRUS MICROCOIL DELIVERY SYSTEM

ApplicantMicrus Endovascular Corporation, San Jose CA, US
DecisionSubstantially Equivalent, Oct 17, 2008
ReceivedSep 18, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K082739

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.