ClearanceBrief
510(k) K811019 ยท KHO Fluorometer, For Clinical Use

LKB 4460 FLUORIMETER

ApplicantLkb Instruments, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 29, 1981
ReceivedApr 15, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K811019

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.