ClearanceBrief
510(k) K141831 ยท DQX Wire, Guide, Catheter

HYDRAVIEW GUIDEWIRE

ApplicantBrivant Limited, Galway, IE
DecisionSubstantially Equivalent, Sep 4, 2014
ReceivedJul 7, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K141831

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.