ClearanceBrief
510(k) K953291 ยท MID System, Test, Anticardiolipin Immunological

QUANTA LITE ACA SCREEN (HRP)

ApplicantInova Diagnostics, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Aug 29, 1995
ReceivedJul 14, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K953291

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.