ClearanceBrief
510(k) K780161 ยท DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control

IMMUNOPEROXIDASE TEST SYS. FOR ANA SETER

ApplicantZeus Scientific, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 7, 1978
ReceivedJan 31, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780161

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.