ClearanceBrief
510(k) K854014 ยท GGP Test, Qualitative And Quantitative Factor Deficiency

ASSERA PLATE IX:AG KIT

ApplicantAmerican Bioproducts Co., Parsippany NJ, US
DecisionSubstantially Equivalent, Jan 3, 1986
ReceivedSep 27, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854014

No recall in the FDA data names this 510(k).

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