ClearanceBrief
510(k) K802579 ยท KHO Fluorometer, For Clinical Use

CYBREX TM FPQ FLUORESCENE POLARIZATION

ApplicantAbbott Laboratories, Abbott Park IL, US
DecisionSubstantially Equivalent, Nov 12, 1980
ReceivedOct 20, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802579

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.