ClearanceBrief
510(k) K895240 ยท KHO Fluorometer, For Clinical Use

DELFIA PLATE FLUOROMETER 1232

ApplicantPharmacia, Inc., Piscataway NJ, US
DecisionSubstantially Equivalent, Oct 4, 1989
ReceivedAug 21, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895240

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.