ClearanceBrief
510(k) K922351 ยท MID System, Test, Anticardiolipin Immunological

QUANTA LITE(TM) IGA ACA

ApplicantInova Diagnostics, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Sep 29, 1992
ReceivedMay 19, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922351

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.