ClearanceBrief
510(k) K831956 ยท CZJ Igd, Antigen, Antiserum, Control

DETERM. SIZE 72 RADIAL-HUMAN IGD

ApplicantKent Laboratories, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 18, 1983
ReceivedJun 17, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831956

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.