ClearanceBrief
510(k) K992452 ยท DOD Gas Chromatography, Amphetamine

RAPIDONE-AMPHETAMINE TEST

ApplicantAmerican Bio Medica Corp., Washington DC, US
DecisionSubstantially Equivalent, Oct 18, 1999
ReceivedJul 22, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K992452

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.