ClearanceBrief
510(k) K820391 ยท LAT Radioimmunoassay, Cannabinoid(S)

ABUSCREEN RADIOIMMUNOASSAY FOR CANNABI

ApplicantHoffmann-La Roche, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 8, 1982
ReceivedFeb 10, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820391

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.