ClearanceBrief
510(k) K820265 ยท DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control

ANA TEST (MOUSE LIVER SUBSTRATE)

ApplicantMeloy Laboratories, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 12, 1982
ReceivedFeb 2, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820265

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.