ClearanceBrief
510(k) K020583 ยท MHI Giardia Spp.

IVD GIARDIA ANTIGEN DETECTION ASSAY MODEL GL-96

ApplicantIvd Research, Inc., Carlsbad CA, US
DecisionSubstantially Equivalent, Sep 17, 2002
ReceivedFeb 21, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K020583

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.