ClearanceBrief
510(k) K884192 ยท LKT Respiratory Syncytial Virus, Antigen, Antibody, Ifa

RSV IFA TEST KIT FOR DIRECT ANTIGEN DETECTION

ApplicantBaxter Diagnostics, Inc., Miami FL, US
DecisionSubstantially Equivalent, Nov 22, 1988
ReceivedOct 6, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884192

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.