ClearanceBrief
510(k) K801037 ยท LCI Automated Radioimmunoassay Systems, For Clinical Use

CENTRIA SYSTEM 2 AUTOMATED METHOD/RIA

ApplicantUnion Carbide Corp., Walker MI, US
DecisionSubstantially Equivalent, May 28, 1980
ReceivedMay 2, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801037

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.