ClearanceBrief
510(k) K854312 ยท GGP Test, Qualitative And Quantitative Factor Deficiency

ASSERACHROM IX:AG

ApplicantAmerican Bioproducts Co., Parsippany NJ, US
DecisionSubstantially Equivalent, Feb 4, 1986
ReceivedOct 28, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854312

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.