ClearanceBrief
510(k) K832020 ยท GKR System, Hemoglobin, Automated

HEMOCUE PHOTOMETER TECHNICAL MANUAL

ApplicantAktiebolaget Leo Diagnostics, Walker MI, US
DecisionSubstantially Equivalent, Oct 28, 1983
ReceivedJun 15, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832020

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.