ClearanceBrief
510(k) K013024 ยท DQX Wire, Guide, Catheter

SELECTIVA GUIDEWIRE

ApplicantNeometrics, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Dec 4, 2001
ReceivedSep 7, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K013024

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.