ClearanceBrief
510(k) K800032 ยท LCQ Fluorescent Immunoassay Gentamicin

FIAX TEST KIT FOR GENTAMICIN QUAN.

ApplicantIntl. Diagnostic Technology, Mchenry IL, US
DecisionSubstantially Equivalent, Jan 23, 1980
ReceivedJan 7, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800032

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.