ClearanceBrief
510(k) K033601 ยท DLJ Calibrators, Drug Specific

LABONE MICRO-PLATE COTININE EIA

ApplicantLabone, Inc., Lenexa KS, US
DecisionSubstantially Equivalent, Feb 10, 2004
ReceivedNov 14, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033601

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.