ClearanceBrief
510(k) K073441 ยท QEZ Aspiration Thrombectomy Catheter

ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039

ApplicantPossis Medical, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Jan 24, 2008
ReceivedDec 7, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K073441

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.