ClearanceBrief
510(k) K892446 ยท KRD Device, Vascular, For Promoting Embolization

SHILEY EQUIPMENT SUPPORT CARTS ESC-002 & ESCB-02

ApplicantShiley, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Jul 14, 1989
ReceivedApr 10, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K892446

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.