ClearanceBrief
510(k) K880742 ยท DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control

NOVA LITE(TM) DSDNA

ApplicantInova Diagnostics, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Mar 25, 1988
ReceivedFeb 24, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880742

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.