ClearanceBrief
510(k) K915351 ยท DQO Catheter, Intravascular, Diagnostic

SHERPA GUIDING CATHETER WITH CATHETER INTRODUCER

ApplicantMedtronics Interventional Vascular, Danvers MA, US
DecisionSubstantially Equivalent, Jun 29, 1992
ReceivedNov 26, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915351

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.