ClearanceBrief
510(k) K832044 ยท DXE Catheter, Embolectomy

SHILEY MULTIPRO CATHETER

ApplicantShiley, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 29, 1983
ReceivedJun 24, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832044

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.