ClearanceBrief
510(k) K860032 ยท DGC Ige, Antigen, Antiserum, Control

TOTAL IGE-IRMA RIA KIT

ApplicantDiagnostic Products Corp., Los Angeles CA, US
DecisionSubstantially Equivalent, Apr 11, 1986
ReceivedJan 6, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860032

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.