ClearanceBrief
510(k) K914022 ยท LFY Enzyme Linked Immunoabsorbent Assay, Varicella-Zoster

SERIOLOGICAL TEST KIT/IGM ANTIBODY VARI-ZOST VIRUS

ApplicantPharmacia Diagnostics, Inc., Columbia MD, US
DecisionSubstantially Equivalent, Jan 27, 1992
ReceivedSep 9, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K914022

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.