ClearanceBrief
510(k) K101729 ยท DQX Wire, Guide, Catheter

NEOWIRE PTA/PTCA GUIDEWIRE

ApplicantNeometrics, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, Sep 23, 2010
ReceivedJun 21, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K101729

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.