ClearanceBrief
510(k) K923320 ยท MID System, Test, Anticardiolipin Immunological

QUANTA LITE ACA SCREEN

ApplicantInova Diagnostics, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Sep 28, 1992
ReceivedJul 7, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923320

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.