ClearanceBrief
510(k) K925951 ยท LRG Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems

READAR

ApplicantAlamar Biosciences Laboratory, Inc., Sacramento CA, US
DecisionSubstantially Equivalent, Aug 31, 1993
ReceivedNov 24, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925951

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.