ClearanceBrief
510(k) K000477 ยท LRM Anti-Dna Antibody (Enzyme-Labeled), Antigen, Control

MDI DS-DNA TEST

ApplicantMicro Detect, Inc., Tustin CA, US
DecisionSubstantially Equivalent, Mar 1, 2000
ReceivedFeb 14, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K000477

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.