ClearanceBrief
510(k) K902953 ยท DQO Catheter, Intravascular, Diagnostic

SOFTOUCH GUIDING CATHETER

ApplicantMallinckrodt Medical, St Louis MO, US
DecisionSubstantially Equivalent, Sep 28, 1990
ReceivedJul 5, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902953

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.