ClearanceBrief
510(k) K882602 ยท GGP Test, Qualitative And Quantitative Factor Deficiency

STACHROM ANTIPLASMIN TEST KIT

ApplicantAmerican Bioproducts Co., Parsippany NJ, US
DecisionSubstantially Equivalent, Sep 2, 1988
ReceivedJun 24, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882602

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.