ClearanceBrief
510(k) K854108 ยท LHL Reagents, Antibody, Legionella, Direct & Indirect Fluorescent

POLYVALENT FLUORESCENT ANTIBODY REAGENTS FOR LEGIO

ApplicantMedical Diagnostic Technologies, Inc., Augusta GA, US
DecisionSubstantially Equivalent, Nov 12, 1985
ReceivedOct 8, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854108

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.