ClearanceBrief
510(k) K870443 ยท LOS

KENZ-CARDICO 1201

ApplicantSuzuken Co., Ltd., Culver City CA, US
DecisionSubstantially Equivalent, Jul 1, 1987
ReceivedFeb 3, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K870443

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.