ClearanceBrief
510(k) K102818 ยท DQX Wire, Guide, Catheter

MICRUS ONE 2 ONE GUIDEWIRE, MICRUS ONE 2 ONE SOFT GUIDEWIRE

ApplicantMicrus Endovascular Corporation, San Jose CA, US
DecisionSubstantially Equivalent, Dec 3, 2010
ReceivedSep 28, 2010
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K102818

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.