ClearanceBrief
510(k) K071342 ยท QEZ Aspiration Thrombectomy Catheter

ANGIOJET ULTRA XPEEDIOR THROMBECTOMY SET, MODEL 105040, 105042, 106552, 105043, 105041, 106553, 105039

ApplicantPossis Medical, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Jul 31, 2007
ReceivedMay 14, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071342

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.