ClearanceBrief
510(k) K780178 ยท DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control

TEST SYS. FOR NDNA ANTIBODY DETERM.

ApplicantZeus Scientific, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 13, 1978
ReceivedFeb 3, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780178

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.