ClearanceBrief
510(k) K051456 ยท JFR Indirect Copper Assay, Ceruloplasmin

SENTINEL CERULOPLASMIN

ApplicantSentinel Ch. Srl, Milano, IT
DecisionSubstantially Equivalent, Oct 21, 2005
ReceivedJun 2, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K051456

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.