ClearanceBrief
510(k) K920012 ยท GGP Test, Qualitative And Quantitative Factor Deficiency

IL TEST(TM) ALPHA-2-ANTIPLASMIN ASSAY SYSTEM

ApplicantInstrumentation Laboratory CO, Lexington MA, US
DecisionSubstantially Equivalent, Aug 12, 1992
ReceivedJan 2, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920012

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.