ClearanceBrief
510(k) K122960 ยท DYB Introducer, Catheter

STEERABLE GUIDING SHEATH, MODEL ADELANTE DESTINO

ApplicantOscor, Inc., Palm Harbor FL, US
DecisionSubstantially Equivalent, Dec 13, 2012
ReceivedSep 25, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K122960

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.