ClearanceBrief
510(k) K120572 ยท OMI Multiplex Flow Immunoassay, T. Gondii, Rubella And Cmv

BIOPLEX 2200 TORC IGG

ApplicantBio-Rad Laboratories, Inc., Benicia CA, US
DecisionSubstantially Equivalent, Mar 26, 2012
ReceivedFeb 27, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K120572

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.