ClearanceBrief
510(k) K060454 ยท DQX Wire, Guide, Catheter

TITAN GUIDEWIRE

ApplicantLake Region Mfg., Inc., Chaska MN, US
DecisionSubstantially Equivalent, Mar 24, 2006
ReceivedFeb 22, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K060454

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.