ClearanceBrief
510(k) K953366 ยท MID System, Test, Anticardiolipin Immunological

QUANTA LITE IGA ACA (HRP)

ApplicantInova Diagnostics, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Sep 1, 1995
ReceivedJul 18, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K953366

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.