ClearanceBrief
510(k) K113162 ยท DQX Wire, Guide, Catheter

SLIDEWIRETM(TRADEMARK PENDING)

ApplicantAcme-Monaco Corp., New Britain CT, US
DecisionSubstantially Equivalent, Jul 20, 2012
ReceivedOct 26, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K113162

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.