ClearanceBrief
510(k) K062809 ยท DQY Catheter, Percutaneous

ADMIRAL XTREME PTA CATHETER

ApplicantInvatec Innovative Technologies, Plymouth MN, US
DecisionSubstantially Equivalent, Oct 18, 2006
ReceivedSep 19, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K062809

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.