ClearanceBrief
510(k) K123792 ยท DQX Wire, Guide, Catheter

HORIZON XVU (FFR)

ApplicantMennen Medical , Ltd., Rohovot, IL
DecisionSubstantially Equivalent, Aug 30, 2013
ReceivedDec 10, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123792

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.