ClearanceBrief
510(k) K120459 ยท DYB Introducer, Catheter

STEERABLE GUIDING SHEATH, MODEL ADELANTE DESTINO

ApplicantOscor, Inc., Palm Harbor FL, US
DecisionSubstantially Equivalent, Jun 29, 2012
ReceivedFeb 15, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K120459

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.