ClearanceBrief
510(k) K971464 ยท DBL Multiple Autoantibodies, Indirect Immunofluorescent, Antigen, Control

IMMUNOSCAN ANTI-GBM QUANTITATIVE KIT

ApplicantEuro-Diagnostica AB, Ringoes NJ, US
DecisionSubstantially Equivalent, Oct 29, 1997
ReceivedApr 22, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K971464

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.