ClearanceBrief
510(k) K990822 ยท DIO Enzyme Immunoassay, Cocaine And Cocaine Metabolites

RAPIDONE - COCAINE TEST

ApplicantAmerican Bio Medica Corp., Washington DC, US
DecisionSubstantially Equivalent, Jul 15, 1999
ReceivedMar 11, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K990822

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.