ClearanceBrief
510(k) K905709 ยท LCP Assay, Glycosylated Hemoglobin

BECKMAN DIATRAC HEMOGLOBIN A ELECTROPHORESIS KIT

ApplicantBeckman Instruments, Inc., Brea CA, US
DecisionSubstantially Equivalent, Sep 23, 1991
ReceivedDec 21, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K905709

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.